Droplet-Based Method And Apparatus For Composite Single-Cell Nucleic Acid Analysis

ABSTRACT

The present invention generally relates to a combination of molecular barcoding and emulsion-based microfluidics to isolate, lyse, barcode, and prepare nucleic acids from individual cells in a high-throughput manner.

RELATED APPLICATIONS AND INCORPORATION BY REFERENCE

This application is a Continuation-in-Part of International ApplicationNumber PCT/US15/49178 filed on Sep. 9, 2015, which published asWO02016/040476 on Mar. 17, 2016 and claims benefit of and priority toU.S. provisional patent application Ser. Nos. 62/048,227 filed Sep. 9,2014; 62/146,642 filed Apr. 13, 2015.

The foregoing applications, and all documents cited therein or duringtheir prosecution (“appin cited documents”) and all documents cited orreferenced in the appin cited documents, and all documents cited orreferenced herein (“herein cited documents”), and all documents cited orreferenced in herein cited documents, together with any manufacturer'sinstructions, descriptions, product specifications, and product sheetsfor any products mentioned herein or in any document incorporated byreference herein, are hereby incorporated herein by reference, and maybe employed in the practice of the invention. More specifically, allreferenced documents are incorporated by reference to the same extent asif each individual document was specifically and individually indicatedto be incorporated by reference.

FEDERAL FUNDING LEGEND

This invention was made with government support under Grant No. HG006193awarded by the National Institutes of Health. The government has certainrights to the invention.

SEQUENCE LISTING

The instant application contains a Sequence Listing which has beensubmitted electronically in ASCII format and is hereby incorporated byreference in its entirety. Said ASCII copy, created March 6, 2017 isnamed 4800992041 SL.txt and is 17.492 bytes in size.

FIELD OF INVENTION

The present invention generally relates to a combination of molecularbarcoding and emulsion-based microfluidics to isolate, lyse, barcode,and prepare nucleic acids from individual cells in a high-throughputmanner.

BACKGROUND OF THE INVENTION

Cells come in different types, sub-types and activity states, whichApplicants classify based on their their shape, location, function, ormolecular profiles, such as the set of RNAs that they express. RNAprofiling is in principle particularly informative, as cells expressthousands of different RNAs. Approaches that measure for example thelevel of every type of RNA have until recently been applied to“homogenized” samples—in which the contents of all the cells are mixedtogether. This has greatly limited our ability to use such techniques tounderstand human tissue function and pathology, for example in thebrain. In the past two years, new technologies have begun emerging toconduct such measurements in single cells, but they are not yet scalableto large numbers of cells, and are very costly. Here, Applicants developa method to profile the RNA content of tens and hundreds of thousands ofindividual human cells, including from brain tissues, quickly andinexpensively. To do so, Applicants use special microfluidic devices toencapsulate each cell in an individual drop, associate the RNA of eachcell with a ‘cell barcode’ unique to that cell/drop, measure theexpression level of each RNA with sequencing, and then use the cellbarcodes to determine which cell each RNA molecule came from. Applicantscan use this approach to better understand almost any biological sample;it is particularly important for understanding samples from any complextissue, for example the retina.

Performing studies that require data resolution at the single cell (orsingle molecule) level can be challenging or cost prohibitive under thebest circumstances. Although techniques or instruments for singlemolecule or single cell analysis exist (e.g., digital polymerase chainreactions (PCR) or Fluidigm C1, respectively), none currently allows ascalable method for dynamically delivering reagents and/or appendingmolecular “information” to individual reactions such that a largepopulation of reactions/assays can be processed and analyzed en massewhile still maintaining the ability to partition results by individualreactions/assays.

Microfluidics involves micro-scale devices that handle small volumes offluids. Because microfluidics may accurately and reproducibly controland dispense small fluid volumes, in particular volumes less than 1 μl,application of microfluidics provides significant cost-savings. The useof microfluidics technology reduces cycle times, shortenstime-to-results, and increases throughput. Furthermore, incorporation ofmicrofluidics technology enhances system integration and automation.Microfluidic reactions are generally conducted in microdroplets. Theability to conduct reactions in microdroplets depends on being able tomerge different sample fluids and different microdroplets. See, e.g., USPatent Publication No. 20120219947.

Droplet microfluidics offers significant advantages for performinghigh-throughput screens and sensitive assays. Droplets allow samplevolumes to be significantly reduced, leading to concomitant reductionsin cost. Manipulation and measurement at kilohertz speeds enable up to108 discrete biological entities (including, but not limited to,individual cells or organelles) to be screened in a single day.Compartmentalization in droplets increases assay sensitivity byincreasing the effective concentration of rare species and decreasingthe time required to reach detection thresholds. Droplet microfluidicscombines these powerful features to enable currently inaccessiblehigh-throughput screening applications, including single-cell andsingle-molecule assays. See, e.g., Guo et al., Lab Chip, 2012, 12,2146-2155.

Citation or identification of any document in this application is not anadmission that such document is available as prior art to the presentinvention.

SUMMARY OF THE INVENTION

The invention particularly relates to a combination of molecularbarcoding and emulsion-based microfluidics to isolate, lyse, barcode,and prepare nucleic acids from individual cells in a high-throughputmanner.

The invention provides a high-throughput single-cell RNA-Seq and/ortargeted nucleic acid profiling (for example, sequencing, quantitativereverse transcription polymerase chain reaction, and the like) where theRNAs from different cells are tagged individually, allowing a singlelibrary to be created while retaining the cell identity of each read. Acombination of molecular barcoding and emulsion-based microfluidics toisolate, lyse, barcode, and prepare nucleic acids from individual cellsin high-throughput is used. Microfluidic devices (for example,fabricated in polydimethylsiloxane), sub-nanoliter reverse emulsiondroplets. These droplets are used to co-encapsulate nucleic acids with abarcoded capture bead. Each bead, for example, is uniquely barcoded sothat each drop and its contents are distinguishable. The nucleic acidsmay come from any source known in the art, such as for example, thosewhich come from a single cell, a pair of cells, a cellular lysate, or asolution. The cell is lysed as it is encapsulated in the droplet. Toload single cells and barcoded beads into these droplets with Poissonstatistics, 100,000 to 10 million such beads are needed to barcode10,000-100,000 cells.

The invention provides a method for creating a single-cell sequencinglibrary comprising: merging one uniquely barcoded mRNA capture microbeadwith a single-cell in an emulsion droplet having a diameter of 75-125μm; lysing the cell to make its RNA accessible for capturing byhybridization onto RNA capture microbead; performing a reversetranscription either inside or outside the emulsion droplet to convertthe cell's mRNA to a first strand cDNA that is covalently linked to themRNA capture microbead; pooling the cDNA-attached microbeads from allcells; and preparing and sequencing a single composite RNA-Seq library.

The invention provides a method for preparing uniquely barcoded mRNAcapture microbeads, which has a unique barcode and diameter suitable formicrofluidic devices comprising: 1) performing reverse phosphoramiditesynthesis on the surface of the bead in a pool-and-split fashion, suchthat in each cycle of synthesis the beads are split into four reactionswith one of the four canonical nucleotides (T, C, G, or A) or uniqueoligonucleotides of length two or more bases; 2) repeating this processa large number of times, at least two, and optimally more than twelve,such that, in the latter, there are more than 16 million unique barcodeson the surface of each bead in the pool. (Seehttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC206447)

Generally, the invention provides a method for preparing a large numberof beads, particles, microbeads, nanoparticles, or the like with uniquenucleic acid barcodes comprising performing polynucleotide synthesis onthe surface of the beads in a pool-and-split fashion such that in eachcycle of synthesis the beads are split into subsets that are subjectedto different chemical reactions; and then repeating this split-poolprocess in two or more cycles, to produce a combinatorially large numberof distinct nucleic acid barcodes. Invention further provides performinga polynucleotide synthesis wherein the synthesis may be any type ofsynthesis known to one of skill in the art for “building” polynucleotidesequences in a step-wise fashion. Examples include, but are not limitedto, reverse direction synthesis with phosphoramidite chemistry orforward direction synthesis with phosphoramidite chemistry. Previous andwell-known methods synthesize the oligonucleotides separately then“glue” the entire desired sequence onto the bead enzymatically.Applicants present a complexed bead and a novel process for producingthese beads where nucleotides are chemically built onto the beadmaterial in a high-throughput manner. Moreover, Applicants generallydescribe delivering a “packet” of beads which allows one to delivermillions of sequences into separate compartments and then screen all atonce.

The invention further provides an apparatus for creating a single-cellsequencing library via a microfluidic system, comprising: aoil-surfactant inlet comprising a filter and a carrier fluid channel,wherein said carrier fluid channel further comprises a resistor; aninlet for an analyte comprising a filter and a carrier fluid channel,wherein said carrier fluid channel further comprises a resistor; aninlet for mRNA capture microbeads and lysis reagent comprising a filterand a carrier fluid channel, wherein said carrier fluid channel furthercomprises a resistor; said carrier fluid channels have a carrier fluidflowing therein at an adjustable or predetermined flow rate; whereineach said carrier fluid channels merge at a junction; and said junctionbeing connected to a mixer, which contains an outlet for drops.

Accordingly, it is an object of the invention not to encompass withinthe invention any previously known product, process of making theproduct, or method of using the product such that Applicants reserve theright and hereby disclose a disclaimer of any previously known product,process, or method. It is further noted that the invention does notintend to encompass within the scope of the invention any product,process, or making of the product or method of using the product, whichdoes not meet the written description and enablement requirements of theUSPTO (35 U.S.C. §112, first paragraph) or the EPO (Article 83 of theEPC), such that Applicants reserve the right and hereby disclose adisclaimer of any previously described product, process of making theproduct, or method of using the product.

It is noted that in this disclosure and particularly in the claimsand/or paragraphs, terms such as “comprises”, “comprised”, “comprising”and the like can have the meaning attributed to it in U.S. Patent law;e.g., they can mean “includes”, “included”, “including”, and the like;and that terms such as “consisting essentially of” and “consistsessentially of” have the meaning ascribed to them in U.S. Patent law,e.g., they allow for elements not explicitly recited, but excludeelements that are found in the prior art or that affect a basic or novelcharacteristic of the invention.

These and other embodiments are disclosed or are obvious from andencompassed by, the following Detailed Description.

BRIEF DESCRIPTION OF THE DRAWINGS

The following detailed description, given by way of example, but notintended to limit the invention solely to the specific embodimentsdescribed, may best be understood in conjunction with the accompanyingdrawings.

FIG. 1 illustrates a microfluidic droplet according to an exemplarydisclosed embodiment. Figure discloses “AAAAAAAAAAAA” and “TTTTTTTTTTTT”as SEQ ID NOS: 17 and 29, respectively.

FIGS. 2A and 2B illustrates an embodiment of the present invention whichbuilds barcodes by split-and-pool synthesis on beads using single basesand a final oligo-dT tail for mRNA capture.

FIGS. 3A-3D illustrate cell barcode sequences approaching thetheoretical level of complexity. FIG. 3D discloses SEQ ID NOS: 18-37,respectively, in order of appearance.

FIG. 4. Microfluidic device illustrating co-encapsulation of cells inPBS injected (once).

FIG. 5. Schematic illustration of microfluidic device

FIG. 6. illustrates sorted drops of interest using the drop-seq methodgenerated from the microfluidic device.

FIGS. 7A-D illustrate molecular barcoding of cellular transcriptomes indroplets.

FIGS. 8A-D illustrate extraction and processing of single-celltranscriptomes by Drop-Seq. FIG. 8D discloses left column sequences asSEQ ID NOS: 38-50 and right column sequences as SEQ ID NOS: 51-63,respectively, in order of appearance.

FIG. 9A-G illustrate critical evaluation of Drop-Seq usingspecies-mixing experiments.

FIG. 10A-C illustrate cell-cycle analysis of HEK and 3T3 cells analyzedby Drop-Seq.

FIG. 11A-F illustrate Ab initio reconstruction of retinal cell typesfrom 44,808 single-cell transcription profiles prepared by Drop-Seq.

FIG. 12A-I Finer-scale expression distinctions among amacrine cells,cones and retinal ganglion cells.

FIG. 13A-C illustrate Ab initio reconstrucstion of human bone marrowcell types from 471 single-cell transcription profiles prepared byDrop-Seq.

FIG. 14A-C illustrate an assessment of the properties of barcodedprimers on the surface of microparticles (beads).

FIG. 15A-E illustrate device design and dissection of technicalcontributions to single-cell impurities in Drop-Seq librarypreparations.

FIG. 16A-F illustrates specificity and sensitivity as a function ofsequencing coverage, evaluated by down-sampling low-depth and high-depthspecies-mixed (HEK/293T) Drop-Seq libraries prepared at a concentrationof 50 cells/μl. (A,B) Analysis of specificity.

FIG. 17A-F illustrates estimation of Drop-Seq expression bias andcapture efficiency.

FIG. 18 illustrates plots of principal components 1-32 of the 44,808retinal cell STAMPs used in analysis.

FIG. 19 illustrates violin plots showing expression of selected markergenes in the 39 retinal cell clusters generated by unsupervised analysisof single-cell gene expression.

FIG. 20 shows the fraction of each cluster composed of cells derivingfrom one of the seven replicates that composed the full 44,808-cell dataset.

FIG. 21 illustrates a schematic representation of Drop-Seq setup.

DETAILED DESCRIPTION OF THE INVENTION

The following detailed description is of example embodiments of thepresently claimed invention with references to the accompanyingdrawings. Such description is intended to be illustrative and notlimiting with respect to the scope of the present invention. Suchembodiments are described in sufficient detail to enable one of ordinaryskill in the art to practice the subject invention, and it will beunderstood that other embodiments may be practiced with some variationswithout departing from the spirit or scope of the subject invention.

The invention provides a nucleotide- or oligonucleotide-adorned beadwherein said bead comprises: a linker; an identical sequence for use asa sequencing priming site; a uniform or near-uniform nucleotide oroligonucleotide sequence; a Unique Molecular Identifier which differsfor each priming site; optionally an oligonucleotide redudant sequencefor capturing polyadenylated mRNAs and priming reverse transcription;and optionally at least one other oligonucleotide barcode which providesan additional substrate for identification.

In an embodiment of the invention, the nucleotide or oligonucleotidesequences on the surface of the bead is a molecular barcode. In an afurther embodiment the barcode ranges from 4 to 1000 nucleotides inlength. In another embodiment, the oligonucleotide sequence forcapturing polyadenylated mRNAs and priming reverse transcription is anoligo dT sequence.

In an embodiment of the invention, the linker is a non-cleavable,straight-chain polymer. In another embodiment, the linker is achemically-cleavable, straight-chain polymer. In a further embodiment,the linker is a non-cleavable, optionally substituted hydrocarbonpolymer. In another embodiment, the linker is a photolabile optionallysubstituted hydrocarbon polymer. In another embodiment, the linker is apolyethylene glycol. In an embodiment, the linker is a PEG-C₃ to PEG-₂₄.

The invention provides a mixture comprising a plurality of nucleotide-or oligonucleotide- adorned beads, wherein said beads comprises: alinker; an identical sequence for use as a sequencing priming site; auniform or near-uniform nucleotide or oligonucleotide sequence; a UniqueMolecular Identifier which differs for each priming site; anoligonucleotide redudant sequence for capturing polyadenylated mRNAs andpriming reverse transcription; and optionally at least one additionaloligonucleotide sequences, which provide substrates for downstreammolecular-biological reactions; wherein the uniform or near-uniformnucleotide or oligonucleotide sequence is the same across all thepriming sites on any one bead, but varies among the oligonucleotides onan individual bead.

In an embodiment of the invention, the nucleotide or oligonucleotidesequence on the surface of the bead is a molecular barcode. In an afurther embodiment the barcode ranges from 4 to 1000 nucleotides inlength. In another embodiment, the oligonucleotide sequence forcapturing polyadenylated mRNAs and priming reverse transcription is anoligo dT sequence.

In an embodiment of the invention, the mixture comprises at least oneoligonucleotide sequences, which provide for substrates for downstreammolecular-biological reactions. In another embodiment, the thedownstream molecular biological reactions are for reverse transcriptionof mature mRNAs; capturing specific portions of the transcriptome,priming for DNA polymerases and/or similar enzymes; or primingthroughout the transcriptome or genome. In an embodiment of theinvention, the additional oligonucleotide sequence comprises a oligio-dTsequence. In another embodiment of the invention, the additionaloligonucleotide sequence comprises a primer sequence. In an embodimentof the invention, the additional oligonucleotide sequence comprises aoligio-dT sequence and a primer sequence.

The invention provides an error-correcting barcode bead wherein saidbead comprises: a linker; an identical sequence for use as a sequencingpriming site; a uniform or near-uniform nucleotide or oligonucleotidesequence which comprises at least a nucleotide base duplicate; a UniqueMolecular Identifier which differs for each priming site; and an anoligonucleotide redudant for capturing polyadenylated mRNAs and primingreverse transcription.

In an embodiment of the invention, the error-correcting barcode beadsfail to hybridize to the mRNA thereby failing to undergo reversetranscription.

The invention also provides a kit which comprises a mixture ofoligonucleotide bound beads and self-correcting barcode beads.

The invention provides a method for creating a single-cell sequencinglibrary comprising: merging one uniquely barcoded RNA capture microbeadwith a single-cell in an emulsion droplet having a diameter from 50 μmto 210 μm; lysing the cell thereby capturing the RNA on the RNA capturemicrobead; breaking droplets and pooling beads in solution; performing areverse transcription reaction to convert the cells' RNA to first strandcDNA that is covalently linked to the RNA capture microbead; orconversely reverse transcribing within droplets and thereafter breakingdroplets and collecting cDNA-attached beads; preparing and sequencing asingle composite RNA-Seq library, containing cell barcodes that recordthe cell-of-origin of each RNA, and molecular barcodes that distinguishamong RNAs from the same cell.

In an embodiment the diameter of the emulsion droplet is between 50-210μm. In a further embodiment, the method wherein the diameter of the mRNAcapture microbeads is from 10 μm to 95 μm. In a further embodiment thediameter of the emulsion droplet is 125 μm.

The invention provides a method for preparing a plurality of beads withunique nucleic acid sequence comprising: performing polynucleotidesynthesis on the surface of the plurality of beads in a pool-and-splitprocess, such that in each cycle of synthesis the beads are split into aplurality of subsets wherein each subset is subjected to differentchemical reactions; repeating the pool-and-split process from anywherefrom 2 cycles to 200 cycles.

In an embodiment of the invention the polynucleotide synthesis isphosphoramidite synthesis. In another embodiment of the invention thethe polynucleotide synthesis is reverse direction phosphoramiditechemistry. In an embodiment of the invention, each subset is subjectedto a different nucleotide. In another embodiment, each subset issubjected to a different canonical nucleotide. In an embodiment of theinvention the method is recepated three, four, or twelve times.

In an embodiment the covalent bond is polyethylene glycol. In anotherembodiment the diameter of the mRNA capture microbeads is from 10 μm to95 μm. In an embodiment, wherein the multiple steps is twelve steps.

In a further embodiment the method further comprises a method forpreparing uniquely barcoded mRNA capture microbeads, which has a uniquebarcode and diameter suitable for microfluidic devices comprising: 1)performing reverse phosphoramidite synthesis on the surface of the beadin a pool-and-split fashion, such that in each cycle of synthesis thebeads are split into four reactions with one of the four canonicalnucleotides (T, C, G, or A); 2) repeating this process a large number oftimes, at least six, and optimally more than twelve, such that, in thelatter, there are more than 16 million unique barcodes on the surface ofeach bead in the pool.

In an embodiment, the diameter of the mRNA capture microbeads is from 10μm to 95 μm.

The invention provides a method for simultaneously preparing a pluralityof nucleotide- or oligonucleotide-adorned beads wherein a uniform,near-uniform, or patterned nucleotide or oligonucleotide sequence issynthesized upon any individual bead while vast numbers of differentnucleotide or oligonucleotide sequences are simultaneously synthesizedon different beads, comprising: forming a mixture comprising a pluralityof beads; separating the beads into subsets; extending the nucleotide oroligonucleotide sequence on the surface of the beads by adding anindividual nucleotide via chemical synthesis; pooling the subsets ofbeads in (c) into a single common pool; repeating steps (b), (c) and (d)multiple times to produce a combinatorially a thousand or morenucleotide or oligonucleotide sequences; and collecting the nucleotide-or oligonucleotide-adorned beads.

In an embodiment of the invention, the nucleotide or oligonucleotidesequence on the surface of the bead is a molecular barcode. In a furtherembodiment, the the pool-and-split synthesis steps occur every 2-10cycles, rather than every cycle.

In an embodiment of the invention, the barcode contains built-in errorcorrection. In another embodiment, the barcode ranges from 4 to 1000nucleotides in length. In embodiment of the invention the thepolynucleotide synthesis is phosphoramidite synthesis. In a furtherembodiment, the polynucleotide synthesis is reverse directionphosphoramidite chemistry. In an embodiment of the invention each subsetis subjected to a different nucleotide. In a further embodiment, one ormore subsets receive a cocktail of two nucleotides. In an embodiment,each subset is subjected to a different canonical nucleotide.

The method provided by the invention contemplates a variety ofembodiments wherein the bead is a microbead, a nanoparticle, or amacrobead. Similarly, the invention contemplates that the theoligonucleotide sequence is a dinucleotide or trinucleotide.

The invention provides a method for simultaneously preparing a thousandor more nucleotide- or oligonucleotide-adorned beads wherein a uniformor near-uniform nucleotide or oligonucleotide sequence is synthesizedupon any individual bead while a plurality of different nucleotide oroligonucleotide sequences are simultaneously synthesized on differentbeads, comprising: forming a mixture comprising a plurality of beads;separating the beads into subsets; extending the nucleotide oroligonucleotide sequence on the surface of the beads by adding anindividual nucleotide via chemical synthesis; pooling the subsets ofbeads in (c) into a single common pool; repeating steps (b), (c) and (d)multiple times to produce a combinatorially large number of nucleotideor oligonucleotide sequences; and collecting the nucleotide- oroligonucleotide-adorned beads; performing polynucleotide synthesis onthe surface of the plurality of beads in a pool-and-split synthesis,such that in each cycle of synthesis the beads are split into aplurality of subsets wherein each subset is subjected to differentchemical reactions; repeating the pool-and-split synthesis multipletimes.

In an embodiment of the invention, the nucleotide or oligonucleotidesequence on the surface of the bead is a molecular barcode. In anembodiment, the pool-and-split synthesis steps occur every 2 to 10cycles, rather than every cycle. In an embodiment, the generatedbardcode contains built-in error correction. In another embodiment, thebarcode ranges from 4 to 1000 nucleotides in length. In embodiment ofthe invention the the polynucleotide synthesis is phosphoramiditesynthesis. In a further embodiment, the polynucleotide synthesis isreverse direction phosphoramidite chemistry. In an embodiment of theinvention each subset is subjected to a different nucleotide. In afurther embodiment, one or more subsets receive a cocktail of twonucleotides. In an embodiment, each subset is subjected to a differentcanonical nucleotide.

The method provided by the invention contemplates a variety ofembodiments wherein the bead is a microbead, a nanoparticle, or amacrobead. Similarly, the invention contemplates that the theoligonucleotide sequence is a dinucleotide or trinucleotide.

The invention further provides an apparatus for creating a compositesingle-cell sequencing library via a microfluidic system, comprising: anoil-surfactant inlet comprising a filter and two carrier fluid channels,wherein said carrier fluid channel further comprises a resistor; aninlet for an analyte comprising a filter and two carrier fluid channels,wherein said carrier fluid channel further comprises a resistor; aninlet for mRNA capture microbeads and lysis reagent comprising a carrierfluid channel; said carrier fluid channels have a carrier fluid flowingtherein at an adjustable and predetermined flow rate; wherein each saidcarrier fluid channels merge at a junction; and said junction beingconnected to a constriction for droplet pinch-off followed by a mixer,which connects to an outlet for drops.

In an embodiment of the apparatus, the analyte comprises a chemicalreagent, a genetically perturbed cell, a protein, a drug, an antibody,an enzyme, a nucleic acid, an organelle like the mitochondrion ornucleus, a cell or any combination thereof. In an embodiment of theapparatus the analyte is a cell. In a further embodiment, the analyte isa mammalian cell. In another embodiment, the analyte of the apparatus iscomplex tissue. In a further embodiment, the cell is a brain cell. In anembodiment of the invention, the cell is a retina cell. In anotherembodiment the cell is a human bone marrow cell. In an embodiment, thecell is a host-pathogen cell.

In an embodiment of the apparatus the lysis reagent comprises an anionicsurfactant such as sodium lauroyl sarcosinate, or a chaotropic salt suchas guanidinium thiocyanate. In an embodiment of the apparatus the filteris consists of square PDMS posts; the filter on the cell channelconsists of such posts with sides ranging between 125-135 μm with aseparation of 70-100 mm between the posts. The filter on theoil-surfactant inlet comprises square posts of two sizes; one with sidesranging between 75-100 μm and a separation of 25-30 μm between them andthe other with sides ranging between 40-50 μm and a separation of 10-15μm. In an embodiment of the apparatus the resistor is serpentine havinga length of 7000-9000 μm, width of 50-75 μm and depth of 100-150 mm. Inan embodiment of the apparatus the channels have a length of 8000-12,000μm for oil-surfactant inlet, 5000-7000 for analyte (cell) inlet, and900-1200 μm for the inlet for microbead and lysis agent. All channelshave a width of 125-250 mm, and depth of 100-150 mm. In anotherembodiment, the width of the cell channel is 125-250 μm and the depth is100-150 μm. In an embodiment of the apparatus the mixer has a length of7000-9000 μm, and a width of 110-140 μm with 35-45° zig-zigs every 150μm. In an embodiment, the width of the mixer is 125 μm. In an embodimentof the apparatus the oil-surfactant is PEG Block Polymer, such asBIORADTM QX200 Droplet Generation Oil. In an embodiment of the apparatusthe carrier fluid is water-glycerol mixture.

A mixture comprising a plurality of microbeads adorned with combinationsof the following elements: bead-specific oligonucleotide barcodescreated by the methods provided; additional oligonucleotide barcodesequences which vary among the oligonucleotides on an indvidual bead andcan therefore be used to differentiate or help identify those individualoligonucleotide molecules; additional oligonucleotide sequences thatcreate substrates for downstream molecular-biological reactions, such asoligo-dT (for reverse transcription of mature mRNAs), specific sequences(for capturing specific portions of the transcriptome, or priming forDNA polymerases and similar enzymes), or random sequences (for primingthroughout the transcriptome or genome). In an embodiment, theindividual oligonucleotide molecules on the surface of any individualmicrobead contain all three of these elements, and the third elementincludes both oligo-dT and a primer sequence.

In another embodiment, a mixture comprising a plurality of microbeads,wherein said microbeads comprise the following elements: at least onebead-specific oligonucleotide barcode obtainable by the processoutlined; at least one additional identifier oligonucleotide barcodesequence, which varies among the oligonucleotides on an individual bead,and thereby assisting in the identification and of the bead specificoligonucleotide molecules; optionally at least one additionaloligonucleotide sequences, which provide substrates for downstreammolecular-biological reactions. In another embodiment the mixturecomprises at least one oligonucleotide sequences, which provide forsubstrates for downstream molecular-biological reactions. In a furtherembodiment the downstream molecular biological reactions are for reversetranscription of mature mRNAs; capturing specific portions of thetranscriptome, priming for DNA polymerases and/or similar enzymes; orpriming throughout the transcriptome or genome. In a further embodimentthe mixture the additional oligonucleotide sequence comprising aoligio-dT sequence. In another embodiment the mixture further comprisesthe additional oligonucleotide sequence comprises a primer sequence. Inanother embodiment the mixture further comprises the additionaloligonucleotide sequence comprising a oligio-dT sequence and a primersequence.

Examples of the labeling substance which may be employed includelabeling substances known to those skilled in the art, such asfluorescent dyes, enzymes, coenzymes, chemiluminescent substances, andradioactive substances. Specific examples include radioisotopes (e.g.,³²P, ¹⁴ _(C,) ¹²⁵I, ³H, and ¹³¹I), fluorescein, rhodamine, dansylchloride, umbelliferone, luciferase, peroxidase, alkaline phosphatase,β-galactosidase, β-glucosidase, horseradish peroxidase, glucoamylase,lysozyme, saccharide oxidase, microperoxidase, biotin, and ruthenium. Inthe case where biotin is employed as a labeling substance, preferably,after addition of a biotin-labeled antibody, streptavidin bound to anenzyme (e.g., peroxidase) is further added.

Advantageously, the label is a fluorescent label. Examples offluorescent labels include, but are not limited to, Atto dyes,4-acetamido-4′-isothiocyanatostilbene-2,2′disulfonic acid; acridine andderivatives: acridine, acridine isothiocyanate;5-(2′-aminoethyl)aminonaphthalene-1-sulfonic acid (EDANS);4-amino-N-[3-vinyl sulfonyl)phenyl]naphthalimide-3,5 disulfonate;N-(4-anilino-1-naphthyl)maleimide; anthranilamide; BODIPY; BrilliantYellow; coumarin and derivatives; coumarin, 7-amino-4-methylcoumarin(AMC, Coumarin 120), 7-amino-4-trifluoromethylcouluarin (Coumaran 151);cyanine dyes; cyanosine; 4′,6-diaminidino-2-phenylindole (DAPI);5′,5″-dibromopyrogallol-sulfonaphthalein (Bromopyrogallol Red);7-diethylamino-3-(4′-isothiocyanatophenyl)-4-methylcoumarin;diethylenetriamine pentaacetate;4,4′-diisothiocyanatodihydro-stilbene-2,2′-disulfonic acid;4,4′-diisothiocyanatostilbene-2,2′-disulfonic acid;5-[dimethylamino]naphthalene-1-sulfonyl chloride (DNS, dansylchloride);4-dimethylaminophenylazophenyl-4′-isothiocyanate (DABITC); eosin andderivatives; eosin, eosin isothiocyanate, erythrosin and derivatives;erythrosin B, erythrosin, isothiocyanate; ethidium; fluorescein andderivatives; 5-carboxyfluorescein (FAM),5-(4,6-dichlorotriazin-2-yl)aminofluorescein (DTAF),2′,7′-dimethoxy-4′5′-dichloro-6-carboxyfluorescein, fluorescein,fluorescein isothiocyanate, QFITC, (XRITC); fluorescamine; IR144;IR1446; Malachite Green isothiocyanate; 4-methylumbelliferoneorthocresolphthalein; nitrotyrosine; pararosaniline; Phenol Red;B-phycoerythrin; o-phthaldialdehyde; pyrene and derivatives: pyrene,pyrene butyrate, succinimidyl 1-pyrene; butyrate quantum dots; ReactiveRed 4 (Cibacron.™. Brilliant Red 3B-A) rhodamine and derivatives:6-carboxy-X-rhodamine (ROX), 6-carboxyrhodamine (R6G), lissaminerhodamine B sulfonyl chloride rhodamine (Rhod), rhodamine B, rhodamine123, rhodamine X isothiocyanate, sulforhodamine B, sulforhodamine 101,sulfonyl chloride derivative of sulforhodamine 101 (Texas Red);N,N,N′,N′ tetramethyl-6-carboxyrhodamine (TAMRA); tetramethyl rhodamine;tetramethyl rhodamine isothiocyanate (TRITC); riboflavin; rosolic acid;terbium chelate derivatives; Cy3; Cy5; Cy5.5; Cy7; IRD 700; IRD 800; LaJolta Blue; phthalo cyanine; and naphthalo cyanine.

The fluorescent label may be a fluorescent protein, such as bluefluorescent protein, cyan fluorescent protein, green fluorescentprotein, red fluorescent protein, yellow fluorescent protein or anyphotoconvertible protein. Colormetric labeling, bioluminescent labelingand/or chemiluminescent labeling may further accomplish labeling.Labeling further may include energy transfer between molecules in thehybridization complex by perturbation analysis, quenching, or electrontransport between donor and acceptor molecules, the latter of which maybe facilitated by double stranded match hybridization complexes. Thefluorescent label may be a perylene or a terrylen. In the alternative,the fluorescent label may be a fluorescent bar code.

In an advantageous embodiment, the label may be light sensitive, whereinthe label is light-activated and/or light cleaves the one or morelinkers to release the molecular cargo. The light-activated molecularcargo may be a major light-harvesting complex (LHCII). In anotherembodiment, the fluorescent label may induce free radical formation.

In an advantageous embodiment, agents may be uniquely labeled in adynamic manner (see, e.g., U.S. provisional patent application Ser. No.61/703,884 filed Sep. 21, 2012). The unique labels are, at least inpart, nucleic acid in nature, and may be generated by sequentiallyattaching two or more detectable oligonucleotide tags to each other andeach unique label may be associated with a separate agent. A detectableoligonucleotide tag may be an oligonucleotide that may be detected bysequencing of its nucleotide sequence and/or by detecting non-nucleicacid detectable moieties to which it may be attached.

The oligonucleotide tags may be detectable by virtue of their nucleotidesequence, or by virtue of a non-nucleic acid detectable moiety that isattached to the oligonucleotide such as but not limited to afluorophore, or by virtue of a combination of their nucleotide sequenceand the nonnucleic acid detectable moiety.

In some embodiments, a detectable oligonucleotide tag may comprise oneor more nonoligonucleotide detectable moieties. Examples of detectablemoieties may include, but are not limited to, fluorophores,microparticles including quantum dots (Empodocles, et al., Nature399:126-130, 1999), gold nanoparticles (Reichert et al., Anal. Chem.72:6025-6029, 2000), microbeads (Lacoste et al., Proc. Natl. Acad. Sci.USA 97(17):9461-9466, 2000), biotin, DNP (dinitrophenyl), fucose,digoxigenin, haptens, and other detectable moieties known to thoseskilled in the art. In some embodiments, the detectable moieties may bequantum dots. Methods for detecting such moieties are described hereinand/or are known in the art.

Thus, detectable oligonucleotide tags may be, but are not limited to,oligonucleotides which may comprise unique nucleotide sequences,oligonucleotides which may comprise detectable moieties, andoligonucleotides which may comprise both unique nucleotide sequences anddetectable moieties.

A unique label may be produced by sequentially attaching two or moredetectable oligonucleotide tags to each other. The detectable tags maybe present or provided in a plurality of detectable tags. The same or adifferent plurality of tags may be used as the source of each detectabletag may be part of a unique label. In other words, a plurality of tagsmay be subdivided into subsets and single subsets may be used as thesource for each tag.

In some embodiments, one or more other species may be associated withthe tags. In particular, nucleic acids released by a lysed cell may beligated to one or more tags. These may include, for example, chromosomalDNA, RNA transcripts, tRNA, mRNA, mitochondrial DNA, or the like. Suchnucleic acids may be sequenced, in addition to sequencing the tagsthemselves, which may yield information about the nucleic acid profileof the cells, which can be associated with the tags, or the conditionsthat the corresponding droplet or cell was exposed to.

The invention described herein enables high throughput and highresolution delivery of reagents to individual emulsion droplets that maycontain cells, organelles, nucleic acids, proteins, etc. through the useof monodisperse aqueous droplets that are generated by a microfluidicdevice as a water-in-oil emulsion. The droplets are carried in a flowingoil phase and stabilized by a surfactant. In one aspect single cells orsingle organellesor single molecules (proteins, RNA, DNA) areencapsulated into uniform droplets from an aqueous solution/dispersion.In a related aspect, multiple cells or multiple molecules may take theplace of single cells or single molecules. The aqueous droplets ofvolume ranging from 1 pL to 10 nL work as individual reactors. Disclosedembodiments provide thousands of single cells in droplets which can beprocessed and analyzed in a single run.

To utilize microdroplets for rapid large-scale chemical screening orcomplex biological library identification, different species ofmicrodroplets, each containing the specific chemical compounds orbiological probes cells or molecular barcodes of interest, have to begenerated and combined at the preferred conditions, e.g., mixing ratio,concentration, and order of combination.

Each species of droplet is introduced at a confluence point in a mainmicrofluidic channel from separate inlet microfluidic channels.Preferably, droplet volumes are chosen by design such that one speciesis larger than others and moves at a different speed, usually slowerthan the other species, in the carrier fluid, as disclosed in U.S.Publication No. US 2007/0195127 and International Publication No. WO2007/089541, each of which are incorporated herein by reference in theirentirety. The channel width and length is selected such that fasterspecies of droplets catch up to the slowest species. Size constraints ofthe channel prevent the faster moving droplets from passing the slowermoving droplets resulting in a train of droplets entering a merge zone.Multi-step chemical reactions, biochemical reactions, or assay detectionchemistries often require a fixed reaction time before species ofdifferent type are added to a reaction. Multi-step reactions areachieved by repeating the process multiple times with a second, third ormore confluence points each with a separate merge point. Highlyefficient and precise reactions and analysis of reactions are achievedwhen the frequencies of droplets from the inlet channels are matched toan optimized ratio and the volumes of the species are matched to provideoptimized reaction conditions in the combined droplets.

Fluidic droplets may be screened or sorted within a fluidic system ofthe invention by altering the flow of the liquid containing thedroplets. For instance, in one set of embodiments, a fluidic droplet maybe steered or sorted by directing the liquid surrounding the fluidicdroplet into a first channel, a second channel, etc. In another set ofembodiments, pressure within a fluidic system, for example, withindifferent channels or within different portions of a channel, can becontrolled to direct the flow of fluidic droplets. For example, adroplet can be directed toward a channel junction including multipleoptions for further direction of flow (e.g., directed toward a branch,or fork, in a channel defining optional downstream flow channels).Pressure within one or more of the optional downstream flow channels canbe controlled to direct the droplet selectively into one of thechannels, and changes in pressure can be effected on the order of thetime required for successive droplets to reach the junction, such thatthe downstream flow path of each successive droplet can be independentlycontrolled. In one arrangement, the expansion and/or contraction ofliquid reservoirs may be used to steer or sort a fluidic droplet into achannel, e.g., by causing directed movement of the liquid containing thefluidic droplet. In another embodiment, the expansion and/or contractionof the liquid reservoir may be combined with other flow-controllingdevices and methods, e.g., as described herein. Non-limiting examples ofdevices able to cause the expansion and/or contraction of a liquidreservoir include pistons.

Key elements for using microfluidic channels to process dropletsinclude: (1) producing droplet of the correct volume, (2) producingdroplets at the correct frequency and (3) bringing together a firststream of sample droplets with a second stream of sample droplets insuch a way that the frequency of the first stream of sample dropletsmatches the frequency of the second stream of sample droplets.Preferably, bringing together a stream of sample droplets with a streamof premade library droplets in such a way that the frequency of thelibrary droplets matches the frequency of the sample droplets.

Methods for producing droplets of a uniform volume at a regularfrequency are well known in the art. One method is to generate dropletsusing hydrodynamic focusing of a dispersed phase fluid and immisciblecarrier fluid, such as disclosed in U.S. Publication No. US 2005/0172476and International Publication No. WO 2004/002627. It is desirable forone of the species introduced at the confluence to be a pre-made libraryof droplets where the library contains a plurality of reactionconditions, e.g., a library may contain plurality of different compoundsat a range of concentrations encapsulated as separate library elementsfor screening their effect on cells or enzymes, alternatively a librarycould be composed of a plurality of different primer pairs encapsulatedas different library elements for targeted amplification of a collectionof loci, alternatively a library could contain a plurality of differentantibody species encapsulated as different library elements to perform aplurality of binding assays. The introduction of a library of reactionconditions onto a substrate is achieved by pushing a premade collectionof library droplets out of a vial with a drive fluid. The drive fluid isa continuous fluid. The drive fluid may comprise the same substance asthe carrier fluid (e.g., a fluorocarbon oil). For example, if a libraryconsists of ten pico-liter droplets is driven into an inlet channel on amicrofluidic substrate with a drive fluid at a rate of 10,000pico-liters per second, then nominally the frequency at which thedroplets are expected to enter the confluence point is 1000 per second.However, in practice droplets pack with oil between them that slowlydrains. Over time the carrier fluid drains from the library droplets andthe number density of the droplets (number/mL) increases. Hence, asimple fixed rate of infusion for the drive fluid does not provide auniform rate of introduction of the droplets into the microfluidicchannel in the substrate. Moreover, library-to-library variations in themean library droplet volume result in a shift in the frequency ofdroplet introduction at the confluence point. Thus, the lack ofuniformity of droplets that results from sample variation and oildrainage provides another problem to be solved. For example if thenominal droplet volume is expected to be 10 pico-liters in the library,but varies from 9 to 11 pico-liters from library-to-library then a10,000 pico-liter/second infusion rate will nominally produce a range infrequencies from 900 to 1,100 droplet per second. In short, sample tosample variation in the composition of dispersed phase for droplets madeon chip, a tendency for the number density of library droplets toincrease over time and library-to-library variations in mean dropletvolume severely limit the extent to which frequencies of droplets may bereliably matched at a confluence by simply using fixed infusion rates.In addition, these limitations also have an impact on the extent towhich volumes may be reproducibly combined. Combined with typicalvariations in pump flow rate precision and variations in channeldimensions, systems are severely limited without a means to compensateon a run-to-run basis. The foregoing facts not only illustrate a problemto be solved, but also demonstrate a need for a method of instantaneousregulation of microfluidic control over microdroplets within amicrofluidic channel.

Combinations of surfactant(s) and oils must be developed to facilitategeneration, storage, and manipulation of droplets to maintain the uniquechemical/biochemical/biological environment within each droplet of adiverse library. Therefore, the surfactant and oil combination must (1)stabilize droplets against uncontrolled coalescence during the dropforming process and subsequent collection and storage, (2) minimizetransport of any droplet contents to the oil phase and/or betweendroplets, and (3) maintain chemical and biological inertness withcontents of each droplet (e.g., no adsorption or reaction ofencapsulated contents at the oil-water interface, and no adverse effectson biological or chemical constituents in the droplets). In addition tothe requirements on the droplet library function and stability, thesurfactant-in-oil solution must be coupled with the fluid physics andmaterials associated with the platform. Specifically, the oil solutionmust not swell, dissolve, or degrade the materials used to construct themicrofluidic chip, and the physical properties of the oil (e.g.,viscosity, boiling point, etc.) must be suited for the flow andoperating conditions of the platform.

Droplets formed in oil without surfactant are not stable to permitcoalescence, so surfactants must be dissolved in the oil that is used asthe continuous phase for the emulsion library. Surfactant molecules areamphiphilic--part of the molecule is oil soluble, and part of themolecule is water soluble. When a water-oil interface is formed at thenozzle of a microfluidic chip for example in the inlet module describedherein, surfactant molecules that are dissolved in the oil phase adsorbto the interface. The hydrophilic portion of the molecule resides insidethe droplet and the fluorophilic portion of the molecule decorates theexterior of the droplet. The surface tension of a droplet is reducedwhen the interface is populated with surfactant, so the stability of anemulsion is improved. In addition to stabilizing the droplets againstcoalescence, the surfactant should be inert to the contents of eachdroplet and the surfactant should not promote transport of encapsulatedcomponents to the oil or other droplets.

A droplet library may be made up of a number of library elements thatare pooled together in a single collection (see, e.g., US PatentPublication No. 2010002241). Libraries may vary in complexity from asingle library element to 1015 library elements or more. Each libraryelement may be one or more given components at a fixed concentration.The element may be, but is not limited to, cells, organelles, virus,bacteria, yeast, beads, amino acids, proteins, polypeptides, nucleicacids, polynucleotides or small molecule chemical compounds. The elementmay contain an identifier such as a label. The terms “droplet library”or “droplet libraries” are also referred to herein as an “emulsionlibrary” or “emulsion libraries.” These terms are used interchangeablythroughout the specification.

A cell library element may include, but is not limited to, hybridomas,B-cells, primary cells, cultured cell lines, cancer cells, stem cells,cells obtained from tissue (e.g., retinal or human bone marrow),peripheral blood mononuclear cell, or any other cell type. Cellularlibrary elements are prepared by encapsulating a number of cells fromone to hundreds of thousands in individual droplets. The number of cellsencapsulated is usually given by Poisson statistics from the numberdensity of cells and volume of the droplet. However, in some cases thenumber deviates from Poisson statistics as described in Edd et al.,“Controlled encapsulation of single-cells into monodisperse picolitredrops.” Lab Chip, 8(8): 1262-1264, 2008. The discrete nature of cellsallows for libraries to be prepared in mass with a plurality of cellularvariants all present in a single starting media and then that media isbroken up into individual droplet capsules that contain at most onecell. These individual droplets capsules are then combined or pooled toform a library consisting of unique library elements. Cell divisionsubsequent to, or in some embodiments following, encapsulation producesa clonal library element.

A variety of analytes may be contemplated for use with the foregoingDrop-Sequencing methods. Examples of cells which are contemplated aremammalian cells, however the invention contemplates a method forprofiling host-pathogen cells. To characterize the expression ofhost-pathogen interactions it is important to grow the host and pathogenin the same cell without multiple opportunities of pathogen infection.

A bead based library element may contain one or more beads, of a giventype and may also contain other reagents, such as antibodies, enzymes orother proteins. In the case where all library elements contain differenttypes of beads, but the same surrounding media, the library elements mayall be prepared from a single starting fluid or have a variety ofstarting fluids. In the case of cellular libraries prepared in mass froma collection of variants, such as genomically modified, yeast orbacteria cells, the library elements will be prepared from a variety ofstarting fluids.

Often it is desirable to have exactly one cell per droplet with only afew droplets containing more than one cell when starting with aplurality of cells or yeast or bacteria, engineered to produce variantson a protein. In some cases, variations from Poisson statistics may beachieved to provide an enhanced loading of droplets such that there aremore droplets with exactly one cell per droplet and few exceptions ofempty droplets or droplets containing more than one cell.

Examples of droplet libraries are collections of droplets that havedifferent contents, ranging from beads, cells, small molecules, DNA,primers, antibodies. Smaller droplets may be in the order of femtoliter(fL) volume drops, which are especially contemplated with the dropletdispensors. The volume may range from about 5 to about 600 fL. Thelarger droplets range in size from roughly 0.5 micron to 500 micron indiameter, which corresponds to about 1 pico liter to 1 nano liter.However, droplets may be as small as 5 microns and as large as 500microns. Preferably, the droplets are at less than 100 microns, about 1micron to about 100 microns in diameter. The most preferred size isabout 20 to 40 microns in diameter (10 to 100 picoliters). The preferredproperties examined of droplet libraries include osmotic pressurebalance, uniform size, and size ranges.

The droplets comprised within the emulsion libraries of the presentinvention may be contained within an immiscible oil which may compriseat least one fluorosurfactant. In some embodiments, the fluorosurfactantcomprised within immiscible fluorocarbon oil is a block copolymerconsisting of one or more perfluorinated polyether (PFPE) blocks and oneor more polyethylene glycol (PEG) blocks. In other embodiments, thefluorosurfactant is a triblock copolymer consisting of a PEG centerblock covalently bound to two PFPE blocks by amide linking groups. Thepresence of the fluorosurfactant (similar to uniform size of thedroplets in the library) is critical to maintain the stability andintegrity of the droplets and is also essential for the subsequent useof the droplets within the library for the various biological andchemical assays described herein. Fluids (e.g., aqueous fluids,immiscible oils, etc.) and other surfactants that may be utilized in thedroplet libraries of the present invention are described in greaterdetail herein.

The present invention provides an emulsion library which may comprise aplurality of aqueous droplets within an immiscible oil (e.g.,fluorocarbon oil) which may comprise at least one fluorosurfactant,wherein each droplet is uniform in size and may comprise the sameaqueous fluid and may comprise a different library element. The presentinvention also provides a method for forming the emulsion library whichmay comprise providing a single aqueous fluid which may comprisedifferent library elements, encapsulating each library element into anaqueous droplet within an immiscible fluorocarbon oil which may compriseat least one fluorosurfactant, wherein each droplet is uniform in sizeand may comprise the same aqueous fluid and may comprise a differentlibrary element, and pooling the aqueous droplets within an immisciblefluorocarbon oil which may comprise at least one fluorosurfactant,thereby forming an emulsion library.

For example, in one type of emulsion library, all different types ofelements (e.g., cells or beads), may be pooled in a single sourcecontained in the same medium. After the initial pooling, the cells orbeads are then encapsulated in droplets to generate a library ofdroplets wherein each droplet with a different type of bead or cell is adifferent library element. The dilution of the initial solution enablesthe encapsulation process. In some embodiments, the droplets formed willeither contain a single cell or bead or will not contain anything, i.e.,be empty. In other embodiments, the droplets formed will containmultiple copies of a library element. The cells or beads beingencapsulated are generally variants on the same type of cell or bead. Inone example, the cells may comprise cancer cells of a tissue biopsy, andeach cell type is encapsulated to be screened for genomic data oragainst different drug therapies. Another example is that 10¹¹ or 10¹⁵different type of bacteria; each having a different plasmid splicedtherein, are encapsulated. One example is a bacterial library where eachlibrary element grows into a clonal population that secretes a varianton an enzyme.

In another example, the emulsion library may comprise a plurality ofaqueous droplets within an immiscible fluorocarbon oil, wherein a singlemolecule may be encapsulated, such that there is a single moleculecontained within a droplet for every 20-60 droplets produced (e.g., 20,25, 30, 35, 40, 45, 50, 55, 60 droplets, or any integer in between).Single molecules may be encapsulated by diluting the solution containingthe molecules to such a low concentration that the encapsulation ofsingle molecules is enabled. In one specific example, a LacZ plasmid DNAwas encapsulated at a concentration of 20 μm after two hours ofincubation such that there was about one gene in 40 droplets, where 10μm droplets were made at 10 kHz per second. Formation of these librariesrely on limiting dilutions.

The present invention also provides an emulsion library which maycomprise at least a first aqueous droplet and at least a second aqueousdroplet within a fluorocarbon oil which may comprise at least onefluorosurfactant, wherein the at least first and the at least seconddroplets are uniform in size and comprise a different aqueous fluid anda different library element. The present invention also provides amethod for forming the emulsion library which may comprise providing atleast a first aqueous fluid which may comprise at least a first libraryof elements, providing at least a second aqueous fluid which maycomprise at least a second library of elements, encapsulating eachelement of said at least first library into at least a first aqueousdroplet within an immiscible fluorocarbon oil which may comprise atleast one fluorosurfactant, encapsulating each element of said at leastsecond library into at least a second aqueous droplet within animmiscible fluorocarbon oil which may comprise at least onefluorosurfactant, wherein the at least first and the at least seconddroplets are uniform in size and comprise a different aqueous fluid anda different library element, and pooling the at least first aqueousdroplet and the at least second aqueous droplet within an immisciblefluorocarbon oil which may comprise at least one fluorosurfactantthereby forming an emulsion library.

One of skill in the art will recognize that methods and systems of theinvention are not limited to any particular type of sample, and methodsand systems of the invention may be used with any type of organic,inorganic, or biological molecule (see, e.g, US Patent Publication No.20120122714). In particular embodiments the sample may include nucleicacid target molecules. Nucleic acid molecules may be synthetic orderived from naturally occurring sources. In one embodiment, nucleicacid molecules may be isolated from a biological sample containing avariety of other components, such as proteins, lipids and non-templatenucleic acids. Nucleic acid target molecules may be obtained from anycellular material, obtained from an animal, plant, bacterium, fungus, orany other cellular organism. In certain embodiments, the nucleic acidtarget molecules may be obtained from a single cell. Biological samplesfor use in the present invention may include viral particles orpreparations. Nucleic acid target molecules may be obtained directlyfrom an organism or from a biological sample obtained from an organism,e.g., from blood, urine, cerebrospinal fluid, seminal fluid, saliva,sputum, stool and tissue. Any tissue or body fluid specimen may be usedas a source for nucleic acid for use in the invention. Nucleic acidtarget molecules may also be isolated from cultured cells, such as aprimary cell culture or a cell line. The cells or tissues from whichtarget nucleic acids are obtained may be infected with a virus or otherintracellular pathogen. A sample may also be total RNA extracted from abiological specimen, a cDNA library, viral, or genomic DNA.

Generally, nucleic acid may be extracted from a biological sample by avariety of techniques such as those described by Maniatis, et al.,Molecular Cloning: A Laboratory Manual, Cold Spring Harbor, N.Y., pp.280-281 (1982). Nucleic acid molecules may be single-stranded,double-stranded, or double-stranded with single-stranded regions (forexample, stem- and loop-structures).

Nucleic acid obtained from biological samples typically may befragmented to produce suitable fragments for analysis. Target nucleicacids may be fragmented or sheared to desired length, using a variety ofmechanical, chemical and/or enzymatic methods. DNA may be randomlysheared via sonication, e.g. Covaris method, brief exposure to a DNase,or using a mixture of one or more restriction enzymes, or a transposaseor nicking enzyme. RNA may be fragmented by brief exposure to an RNase,heat plus magnesium, or by shearing. The RNA may be converted to cDNA.If fragmentation is employed, the RNA may be converted to cDNA before orafter fragmentation. In one embodiment, nucleic acid from a biologicalsample is fragmented by sonication. In another embodiment, nucleic acidis fragmented by a hydroshear instrument. Generally, individual nucleicacid target molecules may be from about 40 bases to about 40 kb. Nucleicacid molecules may be single-stranded, double-stranded, ordouble-stranded with single-stranded regions (for example, stem- andloop-structures).

A biological sample as described herein may be homogenized orfractionated in the presence of a detergent or surfactant. Theconcentration of the detergent in the buffer may be about 0.05% to about10.0%. The concentration of the detergent may be up to an amount wherethe detergent remains soluble in the solution. In one embodiment, theconcentration of the detergent is between 0.1% to about 2%. Thedetergent, particularly a mild one that is nondenaturing, may act tosolubilize the sample. Detergents may be ionic or nonionic. Examples ofnonionic detergents include triton, such as the Triton™ X series(Triton™ X-100 t-Oct-C6H4-—(OCH2-—CH2)xOH, x=9-10, Triton™ X-100R,Triton™ X-114 x=7-8), octyl glucoside, polyoxyethylene(9)dodecyl ether,digitonin, IGEPAL™ CA630 octylphenyl polyethylene glycol,n-octyl-beta-D-glucopyranoside (betaOG), n-dodecyl-beta, Tween™. 20polyethylene glycol sorbitan monolaurate, Tween™ 80 polyethylene glycolsorbitan monooleate, polidocanol, n-dodecyl beta-D-maltoside (DDM),NP-40 nonylphenyl polyethylene glycol, C12E8 (octaethylene glycoln-dodecyl monoether), hexaethyleneglycol mono-n-tetradecyl ether(C14E06), octyl-beta-thioglucopyranoside (octyl thioglucoside, OTG),Emulgen, and polyoxyethylene 10 lauryl ether (C12E10). Examples of ionicdetergents (anionic or cationic) include deoxycholate, sodium dodecylsulfate (SDS), N-lauroylsarcosine, and cetyltrimethylammoniumbromide(CTAB). A zwitterionic reagent may also be used in the purificationschemes of the present invention, such as Chaps, zwitterion 3-14, and3-[(3-cholamidopropyl)dimethylammonio]-1-propanesulfonate. It iscontemplated also that urea may be added with or without anotherdetergent or surfactant.

Lysis or homogenization solutions may further contain other agents, suchas reducing agents. Examples of such reducing agents includedithiothreitol (DTT), β-mercaptoethanol, DTE, GSH, cysteine, cysteamine,tricarboxyethyl phosphine (TCEP), or salts of sulfurous acid.

Size selection of the nucleic acids may be performed to remove veryshort fragments or very long fragments. The nucleic acid fragments maybe partitioned into fractions which may comprise a desired number offragments using any suitable method known in the art. Suitable methodsto limit the fragment size in each fragment are known in the art. Invarious embodiments of the invention, the fragment size is limited tobetween about 10 and about 100 Kb or longer.

In another embodiment, the sample includes individual target proteins,protein complexes, proteins with translational modifications, andprotein/nucleic acid complexes. Protein targets include peptides, andalso include enzymes, hormones, structural components such as viralcapsid proteins, and antibodies. Protein targets may be synthetic orderived from naturally-occurring sources. In one embodiment of theinvention protein targets are isolated from biological samplescontaining a variety of other components including lipids, non-templatenucleic acids, and nucleic acids. In certain embodiments, proteintargets may be obtained from an animal, bacterium, fungus, cellularorganism, and single cells. Protein targets may be obtained directlyfrom an organism or from a biological sample obtained from the organism,including bodily fluids such as blood, urine, cerebrospinal fluid,seminal fluid, saliva, sputum, stool and tissue. Protein targets mayalso be obtained from cell and tissue lysates and biochemical fractions.An individual protein is an isolated polypeptide chain. A proteincomplex includes two or polypeptide chains. Samples may include proteinswith post translational modifications including but not limited tophosphorylation, methionine oxidation, deamidation, glycosylation,ubiquitination, carbamylation, S-carboxymethylation, acetylation, andmethylation. Protein/nucleic acid complexes include cross-linked orstable protein-nucleic acid complexes.

Extraction or isolation of individual proteins, protein complexes,proteins with translational modifications, and protein/nucleic acidcomplexes is performed using methods known in the art.

Methods of the invention involve forming sample droplets. The dropletsare aqueous droplets that are surrounded by an immiscible carrier fluid.Methods of forming such droplets are shown for example in Link et al.(U.S. patent application numbers 2008/0014589, 2008/0003142, and2010/0137163), Stone et al. (U.S. Pat. No. 7,708,949 and U.S. patentapplication number 2010/0172803), Anderson et al. (U.S. Pat. No.7,041,481 and which reissued as RE41,780) and European publicationnumber EP2047910 to Raindance Technologies Inc. The content of each ofwhich is incorporated by reference herein in its entirety.

The present invention relates to systems and methods for manipulatingdroplets within a high throughput microfluidic system. Turning to FIG.1, a microfluid droplet (10) encapsulates a differentiated cell (notshown in the figure). The cell is lysed and its mRNA (20) is hybridizedonto a capture bead containing barcoded oligo dT primers on the surface(30) (40), all inside the droplet. The barcode is covalently attached tothe capture bead via a flexible multi-atom linker like PEG. (50). In apreferred embodiment, the droplets are broken by addition of afluorosurfactant (like perfluorooctanol), washed, and collected. Areverse transcription (RT) reaction is then performed to convert eachcell's mRNA into a first strand cDNA that is both uniquely barcoded andcovalently linked to the mRNA capture bead. Subsequently, a universalprimer via a template switching reaction is amended using conventionallibrary preparation protocols to prepare an RNA-Seq library. Since allof the mRNA from any given cell is uniquely barcoded, a single libraryis sequenced and then computationally resolved to determine which mRNAscame from which cells. In this way, through a single sequencing run,tens of thousands (or more) of distinguishable transcriptomes can besimultaneously obtained.

Turning to FIGS. 2A and 2B, the oligonucleotide sequence generated onthe bead surface is shown in FIG. 2A. During these cycles, beads wereremoved from the synthesis column, pooled, and aliquoted into four equalportions by mass; these bead aliquots were then placed in a separatesynthesis column and reacted with either dG, dC, dT, or dAphosphoramidite. In other instances, dinucleotide, trinucleotides, oroligonucleotides that are greater in length are used, in otherinstances, the oligo-dT tail is replaced by gene specificoligonucleotides to prime specific targets (singular or plural), randomsequences of any length for the capture of all or specific RNAs. Thisprocess was repeated 12 times for a total of 4¹²=16,777,216 uniquebarcode sequences (FIG. 2B). Upon completion of these cycles, 8 cyclesof degenerate oligonucleotide synthesis were performed on all the beads,(the molecular barcode “MBC” in FIG. 2A) followed by 30 cycles of dTaddition. In other embodiments, the degenerate synthesis is omitted,shortened (less than 8 cycles), or extended (more than 8 cycles); inothers, the 30 cycles of dT addition are replaced with gene specificprimers (single target or many targets) or a degenerate sequence.

In FIGS. 3A through 3D, one-thousand cell barcode sequences wereanalysed to determine cell barcode complexity (FIG. 3A).

The aforementioned microfluidic system is regarded as the reagentdelivery system microfluidic library printer or droplet library printingsystem of the present invention (FIG. 4). Droplets (55) are formed assample fluid flows from droplet generator (51) which contains lysisreagent and barcodes through microfluidic outlet channel (52) whichcontains oil (53), towards junction (54). Defined volumes of loadedreagent emulsion, corresponding to defined numbers of droplets, aredispensed on-demand into the flow stream of carrier fluid.

The sample fluid may typically comprise an aqueous buffer solution, suchas ultrapure water (e.g., 18 mega-ohm resistivity, obtained, for exampleby column chromatography), 10 mM Tris HCl and 1 mM EDTA (TE) buffer,phosphate buffer saline (PBS) or acetate buffer. Any liquid or bufferthat is physiologically compatible with nucleic acid molecules can beused. The carrier fluid may include one that is immiscible with thesample fluid. The carrier fluid can be a non-polar solvent, decane(e.g., tetradecane or hexadecane), fluorocarbon oil, silicone oil, aninert oil such as hydrocarbon, or another oil (for example, mineraloil).

In certain embodiments, the carrier fluid may contain one or moreadditives, such as agents which reduce surface tensions (surfactants).Surfactants can include Tween, Span, fluorosurfactants, and other agentsthat are soluble in oil relative to water. In some applications,performance is improved by adding a second surfactant to the samplefluid. Surfactants can aid in controlling or optimizing droplet size,flow and uniformity, for example by reducing the shear force needed toextrude or inject droplets into an intersecting channel. This can affectdroplet volume and periodicity, or the rate or frequency at whichdroplets break off into an intersecting channel. Furthermore, thesurfactant can serve to stabilize aqueous emulsions in fluorinated oilsfrom coalescing.

In certain embodiments, the droplets may be surrounded by a surfactantwhich stabilizes the droplets by reducing the surface tension at theaqueous oil interface. Preferred surfactants that may be added to thecarrier fluid include, but are not limited to, surfactants such assorbitan-based carboxylic acid esters (e.g., the “Span” surfactants,Fluka Chemika), including sorbitan monolaurate (Span 20), sorbitanmonopalmitate (Span 40), sorbitan monostearate (Span 60) and sorbitanmonooleate (Span 80), and perfluorinated polyethers (e.g., DuPont Krytox157 FSL, FSM, and/or FSH). Other non-limiting examples of non-ionicsurfactants which may be used include polyoxyethylenated alkylphenols(for example, nonyl-, p-dodecyl-, and dinonylphenols),polyoxyethylenated straight chain alcohols, polyoxyethylenatedpolyoxypropylene glycols, polyoxyethylenated mercaptans, long chaincarboxylic acid esters (for example, glyceryl and polyglyceryl esters ofnatural fatty acids, propylene glycol, sorbitol, polyoxyethylenatedsorbitol esters, polyoxyethylene glycol esters, etc.) and alkanolamines(e.g., diethanolamine-fatty acid condensates and isopropanolamine-fattyacid condensates).

FIG. 5 illustrates a schematic of an apparatus for creating asingle-cell sequencing library via a microfluidic system. In some cases,the device provides for volume-driven flow, wherein constant volumes areinjected over time. The pressure in fluidic cnannels is a function ofinjection rate and channel dimensions. In an embodiment of the schemeaccording to FIG. 5, the device provides a oil/surfactant inlet (60); aninlet for an analyte (70); a filter (80), an inlet for for mRNA capturemicrobeads and lysis reagent (90); a carrier fluid channel whichconnects the inlets as illustrated in FIG. 5; a resistor (100); aconstriction for droplet pinch-off (101); a mixer (110); and an outletfor drops (120). In an embodiment the invention provides apparatus forcreating a single-cell sequencing library via a microfluidic system,comprising: a oil-surfactant inlet comprising a filter and a carrierfluid channel, wherein said carrier fluid channel further comprises aresistor; an inlet for an analyte comprising a filter and a carrierfluid channel, wherein said carrier fluid channel further comprises aresistor; an inlet for mRNA capture microbeads and lysis reagentcomprising a filter and a carrier fluid channel, wherein said carrierfluid channel further comprises a resistor; said carrier fluid channelshave a carrier fluid flowing therein at an adjustable or predeterminedflow rate; wherein each said carrier fluid channels merge at a junction;and said junction being connected to a mixer, which contains an outletfor drops.

FIG. 6 illustrates a (a) Microfluidic flow scheme for single-cellRNA-seq. Two channels, one carrying cell suspensions, and the othercarrying uniquely barcoded mRNA capture bead, lysis buffer and librarypreparation reagents meet at a junction and is immediatelyco-encapsulated in an inert carrier oil, at the rate of one cell and onebead per drop. In each drop, using the bead's barcode taggedoligonucleotides as cDNA template, each mRNA is tagged with a unique,cell-specific identifier. (b) Drop-Seq library of a mixture of mouse andhuman cells. Each dot represents a unique barcode, and indicates thenumber of genes that could aligned to human (x axis) and mouse (y axis)genomes.

FIG. 7 illustrates molecular barcoding of cellular transcriptomes indroplets. (A) Drop-Seq barcoding schematic. A complex tissue isdissociated into individual cells, which are then encapsulated indroplets together with microparticles (gray circles) that deliverbarcoded primers. Each cell is lysed within a droplet; its mRNAs bind tothe primers on its companion microparticle. The mRNAs arereverse-transcribed into cDNAs, generating a set of beads called“single-cell transcriptomes attached to microparticles” (STAMPs). Thebarcoded STAMPS can then be amplified in pools for high-throughputmRNA-seq to analyze any desired number of individual cells. (B) Sequenceof primers on the microparticle. The primers on all beads contain acommon sequence (“PCR handle”) to enable PCR amplification after STAMPformation. Each microparticle contains more than 10⁸ individual primersthat share the same “cell barcode” (panel C) but have different uniquemolecular identifiers (UMIs), enabling mRNA transcripts to be digitallycounted (panel D). A 30 bp oligo dT sequence (SEQ ID NO:1) is present atthe end of all primer sequences for capture of mRNAs via theirpolyadenylated 3′ ends. (C) Split-and-pool synthesis of the cellbarcode. To generate the cell barcode, the pool of microparticles isrepeatedly split into four equally sized oligonucleotide synthesisreactions, to which one of the four DNA bases is added, and then pooledtogether after each cycle, in a total of 12 split-pool cycles. Thebarcode synthesized on any individual bead reflects that bead's uniquepath through the series of synthesis reactions. The result is a pool ofmicroparticles, each possessing one of 4¹² (16,777,216) possiblesequences on its entire complement of primers. (D) Synthesis of a uniquemolecular identifier (UMI). Following the completion of the“split-and-pool” synthesis cycles, all microparticles are togethersubjected to eight rounds of degenerate synthesis with all four DNAbases available during each cycle, such that each individual primerreceives one of 4⁸ (65,536) possible sequences (UMIs).

FIG. 8 illustrates extraction and processing of single-celltranscriptomes by Drop-Seq. (A) Schematic of single-cell mRNA-Seqlibrary preparation with Drop-Seq. A custom-designed microfluidic devicejoins two aqueous flows before their compartmentalization into discretedroplets. One flow contains cells, and the other flow contains barcodedprimer beads suspended in a lysis buffer. Immediately following dropletformation, the cell is exposed to the lysis agent and releases itsmRNAs, which then hybridize to the primers on the microparticle surface.The droplets are broken by adding a reagent to destabilize the oil-waterinterface (Extended Experimental Procedures), and the microparticlescollected and washed. The mRNAs are then reverse-transcribed in bulk,forming STAMPs, and template switching is used to introduce a PCR handledownstream of the synthesized cDNA (Zhu et al., 2001). (B) Microfluidicdevice used in Drop-Seq. Beads (brown in image), suspended in a lysisagent, enter the device from the central channel; cells enter from thetop and bottom. Laminar flow prevents mixing of the two aqueous inputsprior to droplet formation; this is evident in the image from therefraction of light along the interface of the two flows (see also MovieS1). (C) Molecular elements of a Drop-Seq sequencing library. The firstread yields the cell barcode and UMI. The second, paired readinterrogates sequence from the cDNA (50 bp is typically sequenced,though longer or shorter reads are also possible); this sequence is thenaligned to the genome to determine a transcript's gene of origin. Thecell barcode is used to determine the transcript's cell of origin. (D)In silico reconstruction of thousands of single-cell transcriptomes.Millions of paired-end reads are generated from a Drop-Seq library by ahigh-throughput sequencer (e.g. MiSeq, NextSeq, or HiSeq). The reads arefirst aligned to a reference genome to identify the gene-of-origin ofthe cDNA. Next, reads are organized by their cell barcodes, andindividual UMIs are counted for each gene in each cell (ExtendedExperimental Procedures). The result, shown at far right, is a “digitalexpression matrix” in which each column corresponds to a cell, each rowcorresponds to a gene, and each entry is the integer number oftranscripts detected from that gene, in that cell.

FIG. 9 illustrates critical evaluation of Drop-Seq using species-mixingexperiments. (A,B) Drop-Seq analysis of mixutres of mouse and humancells. Mixtures of human (HEK) and mouse (3T3) cells were analyzed byDrop-Seq at the concentrations shown. The scatter plot shows the numberof human and mouse transcripts associating to each STAMP. Blue dotsindicate STAMPs that were designated from these data as containinghuman-specific sets of transcripts (average of 99% human transcripts);red dots indicate STAMPs inferred to be mouse-specific (average 99%). Atthe lower cell concentration, one STAMP barcode (of 570) associated witha mixture of human and mouse transcripts (panel A, purple). At thehigher cell concentration, about 1.9% of STAMP barcodes associated withmouse-human mixtures (panel B). Data for other cell concentrations and adifferent single-cell analysis platform are in FIGS. S2C and S2D. (C,D)Sensitivity analysis of Drop-Seq at high read-depth. Violin plots showthe distribution of the number of transcripts (B, scored by UMIs) andgenes (C) detected per cell for 54 HEK (human) STAMPs (blue) and 28 3T3(mouse) STAMPs (green) that were sequenced to a mean read depth of737,240 high-quality aligned reads per cell. (E,F) Correlation betweengene expression measurements in Drop-Seq and non-single-cell RNA-seqmethods. Comparison of Drop-Seq gene expression measurements (averagedacross 550 STAMPs) to measurements from bulk RNA analyzed in (E) anmRNA-seq library prepared by an in-solution template switchamplification (TSA) procedure similar to Smart-Seq2 (Picelli et al.,2013) (Extended Experimental Procedures); and (F) Illumina Tru-SeqmRNA-Seq. All comparisons involve RNA derived from the same cell cultureflask (3T3 cells). All expression counts were converted to averagetranscripts per million (ATPM) and plotted as log (1+ATPM). (G)Quantitation of Drop-Seq capture efficiency by ERCC spike-ins. Drop-Seqwas performed with ERCC control synthetic RNAs, spiked in at anestimated concentration of 100,000 ERCC RNA molecules per droplet. 84STAMPs were sequenced at a mean depth of 2.4 million reads, aligned tothe ERCC reference sequences, and UMIs counted for each ERCC species,after applying a stringent down-correction for potential sequencingerrors (Extended Experimental Procedures). For each ERCC RNA speciespresent at at least one molecule per droplet, the predicted number ofmolecules per droplet was plotted in log space (x-axis), versus theactual number of molecules detected per droplet by Drop-Seq, also in logspace (y-axis). The intercept of a regression line, constrained to havea slope of 1 and fitted to the seven highest points, was used toestimate a conversion factor (0.128). A second estimation, using theaverage number of detected transcripts divided by the number of ERCCmolecules used (100,000), yielded a conversion factor of 0.125.

FIG. 10 illustrates cell-cycle analysis of HEK and 3T3 cells analyzed byDrop-Seq. (A) Cell-cycle state of 589 HEK cells (left) and 412 3T3 cells(right) measured by Drop-Seq. Cells were assessed for their progressionthrough the cell cycle by comparison of each cell's global pattern ofgene expression with gene sets known to be enriched in one of fivephases of the cycle (horizontal rows). A phase-specific score wascalculated for each cell across each of these five phases (ExtendedExperimental Procedures), and the cells ordered by their phase scores.(B) Discovery of cell cycle regulated genes. Heat map showing theaverage normalized expression of 544 human and 668 mouse genes found tobe regulated by the cell cycle in the Drop-Seq-sequenced cells. To findgenes that were cell cycle regulated, maximal and minimal expression wascalculated for each gene across a sliding window of the ordered cells,and compared with shuffled cells to obtain a false discovery rate (FDR)(Experimental Procedures). The plotted genes (FDR threshold of 5%) werethen clustered by k-means analysis to identify sets of genes withsimilar expression patterns. Cluster boundaries are represented bydashed gray lines. (C) Representative cell cycle regulated genesdiscovered by Drop-Seq. Selected genes that were found to be cell cycleregulated in both the HEK and 3T3 cell sets. Left, selected genes thatare well-known to be cell cycle regulated. On the right are some genesidentified in this analysis that were not previously known to beassociated with the cell cycle (Experimental Procedures). A completelist of cell cycle regulated genes can be found in Table 4.

FIG. 11 illustrates Ab initio reconstruction of retinal cell types from44,808 single-cell transcription profiles prepared by Drop-Seq. (A)Schematic representation of major cell classes in the retina.Photoreceptors (rods or cones) detect light and pass information tobipolar cells, which in turn contact retinal ganglion cells that extendaxons into other CNS tissues. Amacrine and horizontal cells are retinalinterneurons; Muller glia act as support cells for surrounding neurons.(B) Clustering of 44,808 Drop-Seq single-cell expression profiles into39 retinal cell populations. The plot shows a two-dimensionalrepresentation of global gene expression relationships among 44,808cells; clusters are colored by cell class (colored according to FIG.11A). (C) Differentially expressed genes across 39 retinal cellpopulations. In this heat map, rows correspond to individual genes foundto be selectively upregulated in individual clusters (p<0.01, Bonferronicorrected); columns are individual cells, ordered by cluster (1-39).Clusters>1,000 cells were downsampled to 1,000 cells to prevent themfrom dominating the plot. (D) Gene expression similarity relationshipsamong 39 inferred cell populations. Average gene expression across alldetected genes was calculated for the cells in each of 39 cell clusters,and the relative (Euclidean) distances between gene-expression patternsfor the 39 clusters were represented by a dendrogram. (The dendrogramrepresents global gene expression similarity relationships; it does notrepresent a developmental lineage.) The branches of the dendrogram wereannotated by examining the differential expression of known markers forretina cell classes and types. Twelve examples are shown at right, usingviolin plots to represent the distribution of expression within theclusters. Violin plots for additional genes are in FIG. S6. (E)Representation of experimental replicates in each cell population. tSNEplot from FIG. 8B, with each cell now colored by experimental replicate.Each of the 7 replicates contributes to all 39 cell populations. Cluster36 (arrow), in which these replicates are unevenly represented,expressed markers of fibroblasts which are not native to the retina andare presumably a dissection artifact. (F) Trajectory of amacrineclustering as a function of number of cells analyzed. Three differentdownsampled datasets were generated: (1) 500, (2) 2,000, or (3) 9,451cells (Extended Experimental Procedures). Cells identified as amacrines(clusters 3-23) in the full analysis are here colored by their clusteridentities in that analysis. Analyses of smaller numbers of cellsincompletely distinguished these subpopulations from one another.

FIG. 12. Finer-scale expression distinctions among amacrine cells, conesand retinal ganglion cells. (A) Pan-amacrine markers. The expressionlevels of the six genes identified (Nrxn2, Atplb1, Pax6, Slc32a1,Slc6a1, Elavl3) are represented as dot plots across all 39 clusters;larger dots indicate broader expression within the cluster; deeper reddenotes a higher expression level. (B) Identification of known amacrinetypes among clusters. The twenty-one amacrine clusters consisted oftwelve GABAergic, five glycinergic, one glutamatergic and threenon-GABAergic non-glycinergic clusters. Starburst amacrines wereidentified in cluster 3 by their expression of Chat; excitatoryamacrines were identified by expression of Slc17a8; A-II amacrines wereidentified in cluster 16 by their expression of Gjd2; and SEG amacrineneurons were identified in clusters 17 and 20 by their expression ofEbf3. (C) Nomination of novel candidate markers of amacrinesubpopulations. Each cluster was screened for genes differentiallyexpressed in that cluster relative to all other amacrine clusters(p<0.01, Bonferroni corrected) (McDavid et al., 2013), and filtered forthose with highest relative enrichment. Expression of a single candidatemarker for each cluster is shown across all retinal cell clusters (allgenes differentially expressed in a cluster can be found in Table 6;genes differentially expressed between all cluster pairs can be found inTable 7). (D) Validation of MAF as a marker for a GABAergic amacrinepopulation. Staining of a fixed adult retina from wild-type mice for MAF(panels i, ii, v, and green staining in iv and vii), GAD1 (panels iiiand iv, red staining), and SLC6A9 (panels vi and vii, red staining; MAFstaining is shown in green), demonstrating co-localization of MAF withGAD1, but not SLC6A9. (E) Differential expression of cluster 7 (MAF+)with nearest neighboring amacrine cluster (#6). Average gene expressionwas compared between cells in clusters 6 and 7; sixteen genes (red dots)were identified with >2.8-fold enrichment in cluster 7 (p<10⁻⁹). (F)Validation of PPP1R17 as a marker for an amacrine subpopulation.Staining of a fixed adult retina from Mito-P mice, which express CFP inboth nGnG amacrines and type 1 bipolars (Kay et al., 2011). Asterisks(*) denote bipolar cells labeled in the Mito-P line, while arrowsindicate the nGnG amacrine neurons, which are labeled by both the Mito-Ptransgenic line (red) and the PPP1R17 antibody (green). 85% of CFP+cells were PPP1R17+; 50% of the PPP1R17+ were CFP−, suggesting a secondamacrine type expressing this marker. (G) Differential expression ofcluster 20 (PPP1R17+) with nearest neighboring amacrine cluster (#21).Average gene expression was compared between cells in clusters 20 and21; twelve genes (red dots) were identified with >2.8-fold enrichment incluster 7 (p<10⁻⁹). (H) Differential expression of M-opsin and S-opsincones. Cells in cluster 25 were identified as cone photoreceptors, whichexpress M-opsin (for detecting green light) and/or S-opsin (fordetecting blue light). Average gene expression was compared betweencells expressing M-opsin only (x-axis) and cells-expressing S-opsin only(y-axis). Eight genes showing greater than 2-fold differences inexpression (p<10⁻⁹) are labeled on the plot along with the two opsingenes Opn1mw and Opn1mw. Green points are genes enriched in M-cones,while red points are genes enriched in S-cones. (I) Differentialexpression of melanopsin-positive and negative RGCs. Twenty-four retinalganglion cells expressing Opn4, the gene encoding melanopsin, wereidentified in cluster 2 and average expression was compared betweenthese cells and the remainder of cluster 2. Seven genes were identifiedas differentially expressed (red dots, >2-fold, p<10⁻⁹).

FIGS. 13A-C illustrate Ab initio reconstruction of human bone marrowcell types from 471 single-cell transcription profiles prepared byDrop-Seq. (A) Clustering of single-cell expression profiles into 8 cellclasses. The plot shows a two-dimensional representation (tSNE) ofglobal gene expression relationships among cells; clusters are coloredand labeled by cell class. (B) A heatmap of differentially expressedgenes across 8 cell classes. Rows correspond to individual marker genes;columns are individual cells, ordered by cluster (1-8). (C) Examples ofmarker genes expression (red is high) showed on tSNE map.

FIGS. 14A-C illustrate an assessment of the properties of barcodedprimers on the surface of microparticles (beads). (A) Identification ofindividual bead barcodes in a multiplexed experiment. A syntheticpolyadenylated RNA was reverse transcribed onto the surface of barcodedprimer beads. Eleven of these beads were then manually selected and usedas a template for construction of a sequencing library (ExtendedExperimental Procedures). The library was sequenced on a MiSeq, and thecell barcode sequences gathered and counted. A sharp distinction wasobserved between the numbers of reads carrying the eleventh and twelfthmost abundant 12mers at the barcode position in the sequencing read,demonstrating that cell barcodes from each bead can be recognized fromtheir high representation in the results of a sequencing experiment. (B)Base composition analysis of 12 bp cell barcodes. The sequences of 1,000cell barcodes, ascertained in another sequencing experiment, wereassessed for overall nucleotide and dinucleotide composition. Red dottedlines represent the values for completely random barcode sets that wouldlack any sequence bias. (C) Computational truncation of 12 bp cellbarcodes. The 1,000 cell barcode sequences in (B) were trimmed from the3′ end, and the number of unique barcodes remaining was calculated ateach number of trimmed bases (blue line). The number of unique barcodesat each number of trimmings was compared to a randomly generated set of1,000 12-mers (green line).

FIGS. 15A-E illustrate device design and dissection of technicalcontributions to single-cell impurities in Drop-Seq librarypreparations. (A) Microfluidic co-flow device design. Three inlets—foroil, cell suspension, and microparticles—converge and generate aqueousdroplets composed of equal volume contributions from the cell suspensionand microparticle channels. A winding, bumpy outlet improves mixing ofthe droplets to promote hybridization of released RNAs onto the beads. ACAD file of the device can be found in DataFile 1. (B) Identification ofSTAMPs in a pool of amplified beads. Drop-Seq involves generation ofsingle-cell profiles by diluting cells to poisson-limitingconcentrations in droplets; therefore, the great majority of amplifiedbeads (90-99%) were not exposed to a cell's RNA, only ambient RNA. Toidentify the cell barcodes corresponding to STAMPs, cell barcodes fromthe experiment shown in FIG. 3A are arranged in decreasing order of size(number of reads), and the cumulative fraction of reads is plotted. Aninflection point (vertical dotted line at 570) is observed very close tothe number of cells predicted by Poisson statistics for the counted andaliquoted number of beads (˜500). Confirmation of this inflection pointwas observed by plotting the species specificity of individual STAMPs,and observing a dramatic drop in specificity at the inflection point,indicating the transition from beads that sampled cellular RNA, to thebeads that sampled ambient RNA. (C) Human-mouse experiments on FluidigmC1. Human (HEK) and mouse (3T3) cells were mixed at equal concentrationsand run on two Fluidigm Cl chips according to the manufacturer'sinstructions. Reads were aligned to a joint human-mouse reference inexactly the same analysis pipeline as Drop-Seq. Fifty-six mixed-organismlibraries were identified out of 182, placing a lower bound of 31% oncell-cell doublets. Twelve C1 ports were identified as possessing>1 cellby microscopy, of which five were mixed species by sequencing. (D)Concentration dependence of Drop-Seq library purity. STAMPs wereprepared using a mixture of human (HEK) and mouse (3T3) cells at fourdifferent concentrations (N=1150, 690, 595, and 560 STAMPs for 100cells/μl, 50 cells/μl, 25 cells/μl, and 12.5 cells/μl respectively). Therate of cell doublets was calculated by multiplying by two the number ofmixed species STAMPs; single-cell purity was calculated by summing themean human-cell and mean mouse-cell purities. (E) Single-cell impurityanalysis. Drop-Seq libraries were prepared from combinations of humanand mouse cells pooled at three different stages of DropSeq librarypreparation. In the first condition, human and mouse cells were mixedtogether prior to droplet formation (red violin plot, “Cell Mix”). Inthe second condition, human and mouse cells were separately encapsulatedin droplets, which were then mixed before breaking them and performingsubsequent analyses on the mixture (blue, “Droplet Mix”). In the thirdcondition, human and mouse cells were separately encapsulated indroplets, which were broken in separate reactions and thenreverse-transcribed to form separate pools of covalent STAMPs, whichwere mixed prior to PCR amplification (green, “PCR Mix”). The twentylargest STAMPs from each organism were selected for each of the threeconditions, downsampled to the same read depth, and the organism purityrepresented as violin plots. The black dot is the average organismpurity of the forty STAMPs in each distribution. The cell mixes usedwere diluted to a final concentration of 50 cells/μl in droplets. Fromthese data Applicants estimate that (at this cell concentration) cellsuspension contributes 48% of impurities, RNA transfer after dropletbreakage contributes 40%, and PCR artifacts contribute 12%.

FIGS. 16A-F illustrate specificity and sensitivity as a function ofsequencing coverage, evaluated by down-sampling low-depth and high-depthspecies-mixed (HEK/293T) Drop-Seq libraries prepared at a concentrationof 50 cells/μl. (A,B) Analysis of specificity. Downsampling analysis ofspecies specificity for human-specific STAMPs and mouse-specific STAMPsthat were sequenced at lower read-depth (panel A, 589 human-specific and412 mouse-specific STAMPs) or higher read-depth (panel B, 54 human and28 mouse). (C-F) Analysis of sensitivity. Downsampling analysis ofsingle-cell library sensitivity by average number of genes detected (Cand D) and average number of transcripts detected (E and F) for thelower read-depth Drop-Seq run (C and E) and higher read-depth sequencing(D and F).

FIGS. 17A-F illustrate estimation of Drop-Seq expression bias andcapture efficiency. (A) GC content bias between average gene expressionin Drop-Seq and in-solution template-switch amplification (TSA).Comparison of average gene expression in low GC content genes (<0.4average content, red dots) from a library of 550 3T3 STAMPs, and anmRNA-seq library prepared by an in-solution template switchamplification (TSA) procedure similar to Smart-Seq2 (Picelli et al.,2013) (Extended Experimental Procedures), using RNA derived from thesame cell culture flask that was used in Drop-Seq. (B) GC content biasbetween average gene expression in Drop-Seq and standard mRNA-seq.Comparison of average gene expression in low GC content genes (<0.4average content, red dots) from a library of 550 3T3 STAMPs, and anmRNA-seq library prepared by standard methods (Extended ExperimentalProcedures), using RNA derived from the same cell culture flask that wasused in Drop-Seq. (C) Length bias between average gene expression inDrop-Seq and standard mRNA-seq. Comparison of average gene expression inlong transcripts (>5000 average transcript length, red dots) from alibrary of 550 3T3 STAMPs, and an mRNA-seq library prepared by standardmethods (Extended Experimental Procedures), using RNA derived from thesame cell culture flask that was used in Drop-Seq. The bias observedhere was not found in a comparison of Drop-Seq and in-solution TSA (datanot shown), indicating that this bias is likely the result of templatesuppression PCR, which preferentially amplifies longer fragments (Zhu etal., 2001). (D) Sensitivity estimation by ddPCR. RNA was isolated from aculture of 50,000 HEK cells, and levels of ten genes (ACTB, B2M, CCNB1,GAPDH, EEF2, ENO1, PSMB4, TOP2A, YBX3, and YWHAH) were digitallyquantitated in this bulk solution using RT-ddPCR. These transcriptcounts were then compared to the average number of unique transcriptscounted per cell by Drop-Seq. Error bars show the standard error forindividual ddPCR measurements (horizontal bars, N=3 replicates) oracross STAMPs (vertical bars, N=54). Based upon the mean of these tengene expression measurements, Applicants estimate that DropSeq capturesapproximately 10.7% of cellular mRNAs. (E) Capture efficiency ofbarcoded primer beads. The same barcoded primer beads used in Drop-Seqwere hybridized in solution to purified human brain RNA at aconcentration of 20 ng/μl (Extended Experimental Procedures). The beadswere then spun down and washed three times, and the bound RNA eluted byheating the beads in the presence of water. The concentrations of twomRNA transcripts, GAPDH and ACTB, were measured in each of the fivesteps. Error bars, standard error of the mean.(F) Assessment of barcodedbead primer binding saturation. The same procedure described in (E) wasperformed using three different input RNA concentrations: 20 ng/μl, 50ng/μl and 100 ng/μl. The fraction of input RNA that was eluted off thebeads scaled linearly with input RNA concentration, indicating thathybridization to the beads was not limited by a saturation of mRNAbinding sites.

FIG. 18 illustrates plots of principal components 1-32 of the 44,808retinal cell STAMPs used in analysis. (A) Uncolored PCA plots of 44,808STAMPs; (B) the same PCA plots in (A), but each cell is colored by theirfinal cluster identity, using the colors in FIG. 11B.

FIG. 19 illustrates violin plots showing expression of selected markergenes in the 39 retinal cell clusters generated by unsupervised analysisof single-cell gene expression.

FIG. 20 shows the fraction of each cluster composed of cells derivingfrom one of the seven replicates (prepared over four different days,(Extended Experimental Procedures), that composed the full 44,808-celldata set. The fractions of each replicate are represented as a stackedbarplot. Replicates 1-6 were prepared in an “aggressive mode” ofDrop-Seq (˜90% single-cell, ˜90% purity); replicate 7 was prepared in a“pure mode” (>99% single-cell, 98.6% purity). The stars designate twoimbalanced cluster, #36, corresponding to contaminating fibroblasts thatresult from imperfect retinal dissection.

FIG. 21 illustrates a schematic representation of Drop-Seq setup. Threesyringe pumps, loaded with oil, cells, and beads, respectively, areconnected to the PDMS device in FIG. S2A via flexible tubing. The devicerests on the stage of an inverted microscope so that droplet generationcan be monitored in real-time. Tubing connects the outlet channel to a50 mL conical tube for collection of droplets.

In certain embodiments, the carrier fluid may be caused to flow throughthe outlet channel so that the surfactant in the carrier fluid coats thechannel walls. In one embodiment, the fluorosurfactant can be preparedby reacting the perflourinated polyether DuPont Krytox 157 FSL, FSM, orFSH with aqueous ammonium hydroxide in a volatile fluorinated solvent.The solvent and residual water and ammonia can be removed with a rotaryevaporator. The surfactant can then be dissolved (e.g., 2.5 wt %) in afluorinated oil (e.g., Flourinert (3M)), which then serves as thecarrier fluid.

Activation of sample fluid reservoirs 1012 to produce regent droplets1006 is now described. The disclosed invention is based on the conceptof dynamic reagent delivery (e.g., combinatorial barcoding) via an ondemand capability. The on demand feature may be provided by one of avariety of technical capabilities for releasing delivery droplets to aprimary droplet, as described herein.

An aspect in developing this device will be to determine the flow rates,channel lengths, and channel geometries. Once these designspecifications are established, droplets containing random or specifiedreagent combinations can be generated on demand and merged with the“reaction chamber” droplets containing the samples/cells/substrates ofinterest.

By incorporating a plurality of unique tags into the additional dropletsand joining the tags to a solid support designed to be specific to theprimary droplet, the conditions that the primary droplet is exposed tomay be encoded and recorded. For example, nucleic acid tags can besequentially ligated to create a sequence reflecting conditions andorder of same. Alternatively, the tags can be added independentlyappended to solid support. Non-limiting examples of a dynamic labelingsystem that may be used to bioninformatically record information can befound at U.S. Provisional Patent Application entitled “Compositions andMethods for Unique Labeling of Agents” filed Sep. 21, 2012 and Nov. 29,2012. In this way, two or more droplets may be exposed to a variety ofdifferent conditions, where each time a droplet is exposed to acondition, a nucleic acid encoding the condition is added to the dropleteach ligated together or to a unique solid support associated with thedroplet such that, even if the droplets with different histories arelater combined, the conditions of each of the droplets are remainavailable through the different nucleic acids. Non-limiting examples ofmethods to evaluate response to exposure to a plurality of conditionscan be found at U.S. Provisional Patent Application entitled “Systemsand Methods for Droplet Tagging” filed Sep. 21, 2012.

Applications of the disclosed device may include use for the dynamicgeneration of molecular barcodes (e.g., DNA oligonucleotides,flurophores, etc.) either independent from or in concert with thecontrolled delivery of various compounds of interest (drugs, smallmolecules, siRNA, CRISPR guide RNAs, reagents, etc.). For example,unique molecular barcodes can be created in one array of nozzles whileindividual compounds or combinations of compounds can be generated byanother nozzle array. Barcodes/compounds of interest can then be mergedwith cell-containing droplets. An electronic record in the form of acomputer log file is kept to associate the barcode delivered with thedownstream reagent(s) delivered. This methodology makes it possible toefficiently screen a large population of cells for applications such assingle-cell drug screening, controlled perturbation of regulatorypathways, etc. The device and techniques of the disclosed inventionfacilitate efforts to perform studies that require data resolution atthe single cell (or single molecule) level and in a cost effectivemanner. Disclosed embodiments provide a high throughput and highresolution delivery of reagents to individual emulsion droplets that maycontain cells, nucleic acids, proteins, etc. through the use ofmonodisperse aqueous droplets that are generated one by one in amicrofluidic chip as a water-in-oil emulsion. Hence, the inventionproves advantageous over prior art systems by being able to dynamicallytrack individual cells and droplet treatments/combinations during lifecycle experiments. Additional advantages of the disclosed inventionprovides an ability to create a library of emulsion droplets on demandwith the further capability of manipulating the droplets through thedisclosed process(es). Disclosed embodiments may, thereby, providedynamic tracking of the droplets and create a history of dropletdeployment and application in a single cell based environment.

Droplet generation and deployment is produced via a dynamic indexingstrategy and in a controlled fashion in accordance with disclosedembodiments of the present invention. Disclosed embodiments of themicrofluidic device described herein provides the capability ofmicrodroplets that be processed, analyzed and sorted at a highlyefficient rate of several thousand droplets per second, providing apowerful platform which allows rapid screening of millions of distinctcompounds, biological probes, proteins or cells either in cellularmodels of biological mechanisms of disease, or in biochemical, orpharmacological assays.

A plurality of biological assays as well as biological synthesis arecontemplated for the present invention.

In an advantageous embodiment, polymerase chain reactions (PCR) arecontemplated (see, e.g., US Patent Publication No. 20120219947). Methodsof the invention may be used for merging sample fluids for conductingany type of chemical reaction or any type of biological assay. Incertain embodiments, methods of the invention are used for mergingsample fluids for conducting an amplification reaction in a droplet.Amplification refers to production of additional copies of a nucleicacid sequence and is generally carried out using polymerase chainreaction or other technologies well known in the art (e.g., Dieffenbachand Dveksler, PCR Primer, a Laboratory Manual, Cold Spring Harbor Press,Plainview, N.Y. [1995]). The amplification reaction may be anyamplification reaction known in the art that amplifies nucleic acidmolecules, such as polymerase chain reaction, nested polymerase chainreaction, polymerase chain reaction-single strand conformationpolymorphism, ligase chain reaction (Barany F. (1991) PNAS 88:189-193;Barany F. (1991) PCR Methods and Applications 1:5-16), ligase detectionreaction (Barany F. (1991) PNAS 88:189-193), strand displacementamplification and restriction fragments length polymorphism,transcription based amplification system, nucleic acid sequence-basedamplification, rolling circle amplification, and hyper-branched rollingcircle amplification.

In certain embodiments, the amplification reaction is the polymerasechain reaction. Polymerase chain reaction (PCR) refers to methods by K.B. Mullis (U.S. Pat. Nos. 4,683,195 and 4,683,202, hereby incorporatedby reference) for increasing concentration of a segment of a targetsequence in a mixture of genomic DNA without cloning or purification.The process for amplifying the target sequence includes introducing anexcess of oligonucleotide primers to a DNA mixture containing a desiredtarget sequence, followed by a precise sequence of thermal cycling inthe presence of a DNA polymerase. The primers are complementary to theirrespective strands of the double stranded target sequence.

To effect amplification, primers are annealed to their complementarysequence within the target molecule. Following annealing, the primersare extended with a polymerase so as to form a new pair of complementarystrands. The steps of denaturation, primer annealing and polymeraseextension may be repeated many times (i.e., denaturation, annealing andextension constitute one cycle; there may be numerous cycles) to obtaina high concentration of an amplified segment of a desired targetsequence. The length of the amplified segment of the desired targetsequence is determined by relative positions of the primers with respectto each other, and therefore, this length is a controllable parameter.

Methods for performing PCR in droplets are shown for example in Link etal. (U.S. Patent application numbers 2008/0014589, 2008/0003142, and2010/0137163), Anderson et al. (U.S. Pat. No. 7,041,481 and whichreissued as RE41,780) and European publication number EP2047910 toRaindance Technologies Inc. The content of each of which is incorporatedby reference herein in its entirety.

The first sample fluid contains nucleic acid templates. Droplets of thefirst sample fluid are formed as described above. Those droplets willinclude the nucleic acid templates. In certain embodiments, the dropletswill include only a single nucleic acid template, and thus digital PCRmay be conducted. The second sample fluid contains reagents for the PCRreaction. Such reagents generally include Taq polymerase,deoxynucleotides of type A, C, G and T, magnesium chloride, and forwardand reverse primers, all suspended within an aqueous buffer. The secondfluid also includes detectably labeled probes for detection of theamplified target nucleic acid, the details of which are discussed below.This type of partitioning of the reagents between the two sample fluidsis not the only possibility. In certain embodiments, the first samplefluid will include some or all of the reagents necessary for the PCRwhereas the second sample fluid will contain the balance of the reagentsnecessary for the PCR together with the detection probes.

Primers may be prepared by a variety of methods including but notlimited to cloning of appropriate sequences and direct chemicalsynthesis using methods well known in the art (Narang et al., MethodsEnzymol., 68:90 (1979); Brown et al., Methods Enzymol., 68:109 (1979)).Primers may also be obtained from commercial sources such as OperonTechnologies, Amersham Pharmacia Biotech, Sigma, and Life Technologies.The primers may have an identical melting temperature. The lengths ofthe primers may be extended or shortened at the 5′ end or the 3′ end toproduce primers with desired melting temperatures. Also, the annealingposition of each primer pair may be designed such that the sequence and,length of the primer pairs yield the desired melting temperature. Thesimplest equation for determining the melting temperature of primerssmaller than 25 base pairs is the Wallace Rule (Td=2(A+T)+4(G+C)).Computer programs may also be used to design primers, including but notlimited to Array Designer Software (Arrayit Inc.), Oligonucleotide ProbeSequence Design Software for Genetic Analysis (Olympus Optical Co.),NetPrimer, and DNAsis from Hitachi Software Engineering. The TM (meltingor annealing temperature) of each primer is calculated using softwareprograms such as Oligo Design, available from Invitrogen Corp.

A droplet containing the nucleic acid is then caused to merge with thePCR reagents in the second fluid according to methods of the inventiondescribed above, producing a droplet that includes Taq polymerase,deoxynucleotides of type A, C, G and T, magnesium chloride, forward andreverse primers, detectably labeled probes, and the target nucleic acid.

Once mixed droplets have been produced, the droplets are thermal cycled,resulting in amplification of the target nucleic acid in each droplet.In certain embodiments, the droplets are flowed through a channel in aserpentine path between heating and cooling lines to amplify the nucleicacid in the droplet. The width and depth of the channel may be adjustedto set the residence time at each temperature, which may be controlledto anywhere between less than a second and minutes.

In certain embodiments, the three temperature zones are used for theamplification reaction. The three temperature zones are controlled toresult in denaturation of double stranded nucleic acid (high temperaturezone), annealing of primers (low temperature zones), and amplificationof single stranded nucleic acid to produce double stranded nucleic acids(intermediate temperature zones). The temperatures within these zonesfall within ranges well known in the art for conducting PCR reactions.See for example, Sambrook et al. (Molecular Cloning, A LaboratoryManual, 3rd edition, Cold Spring Harbor Laboratory Press, Cold SpringHarbor, N.Y., 2001).

In certain embodiments, the three temperature zones are controlled tohave temperatures as follows: 95° C. (TH), 55° C. (TL), 72° C. (TM). Theprepared sample droplets flow through the channel at a controlled rate.The sample droplets first pass the initial denaturation zone (TH) beforethermal cycling. The initial preheat is an extended zone to ensure thatnucleic acids within the sample droplet have denatured successfullybefore thermal cycling. The requirement for a preheat zone and thelength of denaturation time required is dependent on the chemistry beingused in the reaction. The samples pass into the high temperature zone,of approximately 95° C., where the sample is first separated into singlestranded DNA in a process called denaturation. The sample then flows tothe low temperature, of approximately 55° C., where the hybridizationprocess takes place, during which the primers anneal to thecomplementary sequences of the sample. Finally, as the sample flowsthrough the third medium temperature, of approximately 72° C., thepolymerase process occurs when the primers are extended along the singlestrand of DNA with a thermostable enzyme.

The nucleic acids undergo the same thermal cycling and chemical reactionas the droplets pass through each thermal cycle as they flow through thechannel. The total number of cycles in the device is easily altered byan extension of thermal zones. The sample undergoes the same thermalcycling and chemical reaction as it passes through N amplificationcycles of the complete thermal device.

In other embodiments, the temperature zones are controlled to achievetwo individual temperature zones for a PCR reaction. In certainembodiments, the two temperature zones are controlled to havetemperatures as follows: 95° C. (TH) and 60° C. (TL). The sample dropletoptionally flows through an initial preheat zone before entering thermalcycling. The preheat zone may be important for some chemistry foractivation and also to ensure that double stranded nucleic acid in thedroplets is fully denatured before the thermal cycling reaction begins.In an exemplary embodiment, the preheat dwell length results inapproximately 10 minutes preheat of the droplets at the highertemperature.

The sample droplet continues into the high temperature zone, ofapproximately 95° C., where the sample is first separated into singlestranded DNA in a process called denaturation. The sample then flowsthrough the device to the low temperature zone, of approximately 60° C.,where the hybridization process takes place, during which the primersanneal to the complementary sequences of the sample. Finally thepolymerase process occurs when the primers are extended along the singlestrand of DNA with a thermostable enzyme. The sample undergoes the samethermal cycling and chemical reaction as it passes through each thermalcycle of the complete device. The total number of cycles in the deviceis easily altered by an extension of block length and tubing.

After amplification, droplets may be flowed to a detection module fordetection of amplification products. The droplets may be individuallyanalyzed and detected using any methods known in the art, such asdetecting for the presence or amount of a reporter. Generally, thedetection module is in communication with one or more detectionapparatuses. The detection apparatuses may be optical or electricaldetectors or combinations thereof. Examples of suitable detectionapparatuses include optical waveguides, microscopes, diodes, lightstimulating devices, (e.g., lasers), photo multiplier tubes, andprocessors (e.g., computers and software), and combinations thereof,which cooperate to detect a signal representative of a characteristic,marker, or reporter, and to determine and direct the measurement or thesorting action at a sorting module. Further description of detectionmodules and methods of detecting amplification products in droplets areshown in Link et al. (U.S. patent application numbers 2008/0014589,2008/0003142, and 2010/0137163) and European publication numberEP2047910 to Raindance Technologies Inc.

In another embodiment, examples of assays are ELISA assays (see, e.g.,US Patent Publication No. 20100022414). The present invention providesanother emulsion library which may comprise a plurality of aqueousdroplets within an immiscible fluorocarbon oil which may comprise atleast one fluorosurfactant, wherein each droplet is uniform in size andmay comprise at least a first antibody, and a single element linked toat least a second antibody, wherein said first and second antibodies aredifferent. In one example, each library element may comprise a differentbead, wherein each bead is attached to a number of antibodies and thebead is encapsulated within a droplet that contains a different antibodyin solution. These antibodies may then be allowed to form “ELISAsandwiches,” which may be washed and prepared for a ELISA assay.Further, these contents of the droplets may be altered to be specificfor the antibody contained therein to maximize the results of the assay.

In another embodiment, single-cell assays are also contemplated as partof the present invention (see, e.g., Ryan et al., Biomicrofluidics 5,021501 (2011) for an overview of applications of microfluidics to assayindividual cells). A single-cell assay may be contemplated as anexperiment that quantifies a function or property of an individual cellwhen the interactions of that cell with its environment may becontrolled precisely or may be isolated from the function or propertyunder examination. The research and development of single-cell assays islargely predicated on the notion that genetic variation causes diseaseand that small subpopulations of cells represent the origin of thedisease. Methods of assaying compounds secreted from cells, subcellularcomponents, cell-cell or cell-drug interactions as well as methods ofpatterning individual cells are also contemplated within the presentinvention

In other embodiments, chemical prototyping and synthetic chemicalreactions are also contemplated within the methods of the invention.

Although the present invention and its advantages have been described indetail, it should be understood that various changes, substitutions andalterations can be made herein without departing from the spirit andscope of the invention as defined in the appended claims.

The present invention will be further illustrated in the followingExamples which are given for illustration purposes only and are notintended to limit the invention in any way.

EXAMPLES Example 1

In this protocol, uniquely barcoded beads are synthesized for use asprimers for reverse transcription. Beads begin first with having a fixedsequence (SMT A in FIG. 2A) synthesized on the surface, which is used asa priming site for downstream PCR. Next, beads are split and pooled intofour equal reaction vessels a total of 12 times, to generate 4̂12 uniquebarcode sequences that are unique to each bead (FIG. 2B). This 12 bpregion will serve as the cell barcode, since it is specific to eachbead. Next, the beads are all pooled together for 8 rounds of degeneratesynthesis with all four bases; this 8 bp region is a “molecular barcode”and will tag each mRNA uniquely, so that each mRNA molecule in a cellcan be digitally counted. Finally, 30 dT bases (SEQ ID NO:1) aresynthesized, which serves as the capture region for the polyadenylatedtails of mRNAs (referred to frequently in the literature as “oligo dT”).

Synthesis of Uniquely Barcoded Beads

Toyopearl HW-65S resin was purchased from Tosoh Biosciences, inc.Surface hydroxyls were reacted with a PEG derivative to generate an18-carbon long, flexible-chain linker. The derivatized bead was thenused as a solid support for reverse 5′->3′ phosphoramidite synthesis onan Expedite 8909 DNA/RNA synthesizer using DNA Synthesis 10 μmol cyclescale and a coupling time of 3 minutes. Amidites used were:N⁶-Benzoyl-3′-O-DMT-2′-deoxyadenosine-5′-cyanoethyl-N,N-diisopropyl-phosphoramidite(dA-N-Bz);N⁴-Acetyl-3′-O-DMT-2′-deoxy-cytidine-5′-cyanoethyl-N,N-diisopropyl-phosphoramidite(dC-N-Ac);N²-DMF-3′-O-DMT-2′-deoxyguanosine-5′-cyanoethyl-N,N-diisopropylphosphoramidite(dG-N-DMF);3′-O-DMT-2′-deoxythymidine-5′-cyanoethyl-N,N-diisopropylphosphoramidite;and3′-O-DMT-2′-deoxyuridine-5′-cyanoethyl-N,N-diisopropylphosphoramidite.Acetic anhydride and N-methylimidazole were used in the capping step;ethylthiotetrazole was used in the activation step; iodine was used inthe oxidation step, and dichloroacetic acid was used in the deblockingstep. The oligonucleotide sequence generated on the bead surface isshown in FIG. 2A. A constant sequence (“SMT A in figure) for use as aPCR handle, is synthesized. Then, 12 cycles of pool-and-splitphosphoramidite synthesis are performed (the cell barcode or “CBC” inFIG. 2A). During these cycles, beads were removed from the synthesiscolumn, pooled, and aliquoted into four equal portions by mass; thesebead aliquots were then placed in a separate synthesis column andreacted with either dG, dC, dT, or dA phosphoramidite. This process wasrepeated 12 times for a total of 4̂12=16,777,216 unique barcode sequences(FIG. 2B). Upon completion of these cycles, 8 cycles of degenerateoligonucleotide synthesis were performed on all the beads, (themolecular barcode “MBC” in FIG. 2A) followed by 30 cycles of dTaddition.

Characterization of Beads

1) Determination of bead binding capacity for polyadenylated RNA.Saturating quantities (100 pmol per 20,000 beads) of polyadenylatedsynthetic RNA was annealed to barcodes beads in 2×SSC for 5 min. Thebeads were then washed 3× with 200 ul of 1× TE+0.01% Tween, andresuspended in 10 ul of TE. The beads were then heated at 65 C for 5min, and a ul of the supernatant was quantified on the NanodropSpectrophotometer at 260 nm.

2) Determination of quality and homogeneity of cell barcode sequences.Synthetic RNA was flowed into a 125 μl microfluidic co-flow dropletgeneration device at a concentration of 0.2 uM. The other flow containeda 2× reverse transcription mix. The droplets were incubated at 42° C.for 30 minutes, then broken. 11 beads were picked to a PCR tube andamplified with 17 cycles of PCR. The amplicon product was purified andquantified on the Bioanalyzer 2100, then sequenced on MiSeq. The cellbarcode sequences were extracted and collapsed at edit distance 1 toobtain FIG. 3B.

3) Determination of cell barcode complexity. 1000 cell barcode sequenceswere analyzed for base composition (FIG. 2C), dinucleotide composition(FIG. 2D), and were serially trimmed from the 3′ end and checked forduplicate sequences (FIG. 2E). In all three analyses, the empirical cellbarcodes displayed complexity that was only slightly below thetheoretical limit of their complexity given their length (4̂12 uniquesequences).

DropSeq Protocol

1. Reagents for preparing cells and beads for processing: Lysis Buffer(per mL): 680 μl H₂O 120 μl 50% Ficoll  10 μl 20% Sarkosyl  40 μl EDTA100 μl 2M Tris pH 7.5  50 μl 1M DTT (add at the end)

PBS-BSA: 995 μl cold 1x PBS  5 μl NEB BSA (20 mg/ml)

Prepare the oil and device: Load oil into a 10 mL syringe. Affix needle(27G1/2) and tubing (PE-2), push oil through the tubing to the end, andload into pump. Place the tubing end in the left-most channel of a cleandevice (See FIG. 6, all features on device are 125 μm deep).

Cell Culture

Human 293 T cells were purchased as well as murine NIH/3T3 cells. 293Tand 3T3 cells were grown in DMEM supplemented with 10% FBS and 1%penicillin-streptomycin.

Cells were grown to a confluence of 30-60% and treated with TrypLE forfive min, quenched with equal volume of growth medium, and spun down at300×g for 5 min. The supernatant was removed, and cells were resuspendedin 1 mL of 1× PBS+0.2% BSA and re-spun at 300×g for 3 min. Thesupernatant was again removed, and the cells re-suspended in 1 mL of 1×PBS, passed through a 40-micron cell strainer, and counted. ForDrop-Seq, cells were diluted to the final concentration in 1× PBS+200μg/mL BSA.

Generation of Whole Retina Suspensions

Single cell suspensions were prepared from P14 mouse retinas by adaptingpreviously, l described methods for purifying retinal ganglion cellsfrom rat retina (Barres et al., 1988). Briefly, mouse retinas weredigested in a papain solution (40U papain/10 mL DPBS) for 45 minutes.Papain was then neutralized in a trypsin inhibitor solution (0.15%ovomucoid in DPBS) and the tissue was triturated to generate a singlecell suspension. Following trituration, the cells were pelleted andresuspended and the cell suspension was filtered through a 20pm Nitexmesh filter to eliminate any clumped cells and this suspension was thenused for Drop-Seq. The cells were then diluted in DPBS+0.2% BSA toeither 200 cells/μl (replicates 1-6) or 30 cells/μl (replicate 7).

Retina suspensions were processed through Drop-Seq on four separatedays. One library was prepared on day 1 (replicate 1); two libraries onday 2 (replicates 2 and 3); three libraries on day 3 (replicates 4-6);and one library on day 4 (replicate 7, high purity). To replicates 4-6,human HEK cells were spiked in at a concentration of 1 cell/μl (0.5%)but the wide range of cell sizes in the retina data made it impossibleto calibrate single-cell purity or doublets using the cross-speciescomparison method. Each of the seven replicates was sequencedseparately.

Preparation of Beads

Beads (either Barcoded Bead SeqA or Barcoded Bead SeqB) were washedtwice with 30 mL of 100% EtOH and twice with 30 mL of TE/TW (10 mM TrispH 8.0, 1 mM EDTA, 0.01% Tween). The bead pellet was resuspended in 10mL TE/TW and passed through a 100 μm filter into a 50 mL Falcon tube forlong-term storage at 4° C. The stock concentration of beads (inbeads/μL) was assessed using a Fuchs-Rosenthal cell counter. ForDrop-Seq, an aliquot of beads was removed from the stock tube, washed in500 μl of Drop-Seq Lysis Buffer (DLB, 200 mM Tris pH 7.5, 6% FicollPM-400, 0.2% Sarkosyl, 20 mM EDTA), then resuspended in the appropriatevolume of DLB +50 mM DTT for a bead concentration of 100 beads/μL.

Cell lysis and mRNA hybridization to beads on the microfluidicdevice. 1) Surfactant-containing oil; 2) cells suspended in aqueoussolution (like PBS); and 3) barcoded beads suspended in a lysis agent(i.e., detergent). Cells and beads are flowed simultaneously into thedevice, where they unite and form droplets. Once inside the droplets,the cells lyse, RNA is released, and captured onto the surface of thebarcoded bead by hybridization

Syringe Pump: 14,000 μl/hr for oil; 4,100 μl/hr each for beads andcells; collect droplets in 50 mL falcon tubes; use 1 falcon tube per1500 μl of aqueous solution (750 μl of each flow).

3. Post-device processing of RNA-hybridized beads into cDNA

BREAK DROPLETS: Immediately after completing droplet generation, removeoil from the bottom. Add 30 mL of room temperature 6x SSC. Shake. 6x SSCAdd 600 μl of Perfluorooctanol (PFO). Mix well. Spin at 1000xg for 1minute. Remove all but ~2-3 mL of liquid. Add 30 mL 6x SSC and spinagain. Remove all but <1 mL of liquid. Transfer to eppendorf tubes andspin down to remove the supernatant. Wash 2x with 1 mL of 6x SSC thenonce with 300 μl of 5x RT buffer.

Reverse transcription: RT Mix (per 90,000 beads): 75 μl H₂O 40 μl Maxima5x RT Buffer 40 μl 20% Ficoll PM-400 20 μl 10 mM dNTPs (Clontech)  5 μlRNase Inhibitor (Lucigen) 10 μl 50 μM Template Switch Oligo 10 μl MaximaH-RT (add just before starting RT)

Incubate and rotate at: RT for 30 minutes 42° C. for 90 minutes

Wash Wash beads once with TE + 0.5% SDS, then 2x with TE + TW (0.02%),then add 1 mL 10 mm Tris pH 7.5.

Microfluidic device is fabricated using polydimethylsiloxane (PDMS) froma master made of SU8 photo-resist1. The PDMS device is thenplasma-treated to bond with a glass microscope slide (75 mm×50 mm×1mm).Since we work with a continuous oil phase, the channels are renderedhydrophobic by flowing in Aquapel (Rider, Mass., USA) through the oilinlet and flushing out the excess fluid through the remaininginlets/outlets using pressurized air. See McDonald, J. C. et al.Fabrication of microfluidic systems in poly(dimethylsiloxane).Electrophoresis 21, 27 (2000).

Example 2 Genome-Wide Expression Profiling of Thousands of IndividualCells using Nanoliter Droplets

Disease takes place within complex tissues, made of different types ofcells, and (almost) never involves a single cell acting on its own:cells interact with each other constantly, making collective decisions,coordinating dynamic changes and working together. In normal tissue thisresults in homeostasis; in disease a malfunction in one or moreinteractions can lead to or exacerbate pathology.

Cells, the basic units of biological structure and function, varybroadly in type and state. Single cell genomics can characterize cellidentity and function, but limitations of ease and scale have preventedits broad application. Here Applicants describe Drop-Seq, a strategy forquickly profiling thousands of individual cells by separating them intonanoliter-sized aqueous droplets, applying a different barcode to eachcell's RNAs, and sequencing them all together. Drop-Seq analyzes mRNAtranscripts from thousands of individual cells while rememberingtranscripts' cell of origin. Applicants analyzed transcriptomes from44,808 mouse retinal cells and defined thirty-nine distinct cellpopulations, recapitulating the major retinal cell classes, identifyingcandidate markers of subtypes, and profiling gene expression in each.Applicants also analyzed 471 human bone marrow cells and defined eightdistinct cell populations. Drop-Seq will accelerate biological discoveryby enabling routine transcriptional profiling at single-cell resolution.

Individual cells are the building blocks of tissues, organs, andorganisms. Each tissue contains cells of many types, and cells of eachtype can switch among biological states. The number of cell types in atissue can be over 100, and the number of states per cell is unknown.Because each type and state has unique functional capacities, responsesand molecular compositions, it will be necessary to ascertain cell typesand states to understand tissue physiology, developmental processes, anddisease.

In most biological systems, Applicants' knowledge of cellular diversityis incomplete. For example, the cell-type complexity of the brain isunknown and widely debated (Luo et al., 2008; Petilla InterneuronNomenclature et al., 2008). Many important but rare cell populationslikely are undiscovered. Such rare types can play critical roles.Purkinje neurons, for example, are essential to brain function thoughthey comprise less than 0.05% of neurons in the cerebellum (Andersen etal., 1992). Discovering a rare cell population may require analyzinglarge numbers of cells, ideally in an unbiased manner.

A major determinant of each cell's function is its transcriptionalprogram. Recent advances now enable mRNA-seq analysis of individualcells (Kurimoto et al., 2006; Tang et al., 2009). HoFIGS.ver, currentmethods of preparing cells for profiling are applied to hundreds(Hashimshony et al., 2012; Islam et al., 2012; Picelli et al., 2013;Pollen et al., 2014; Shalek et al., 2014) or (with automation) a fewthousand cells (Jaitin et al., 2014), typically after first separatingthe cells by sorting (Shalek et al., 2013), picking (Hashimshony et al.,2012), or microfluidics (Shalek et al., 2014), and then amplifying eachcell's transcriptome in its own well or microfluidics chamber. Scalableapproaches will be needed to characterize complex tissues with many celltypes and states, under diverse conditions and perturbations. Profilinglarge numbers of cells may also be important for distinguishing noisefrom biologically meaningful patterns (sometimes involving small numbersof genes) that recur in many cells (Grun et al., 2014; Kharchenko etal., 2014).

The major obstacles to large-scale single-cell studies have been thecost and time involved in preparing large numbers of individual cellsfor sequencing. Here, Applicants describe a way to circumvent thisobstacle by encapsulating thousands of individual cells in tiny“droplets”—nanoliter-scale aqueous compartments formed when water andoil mix—then barcoding the RNAs in each droplet in order to poolthousands of barcoded single-cell transcriptomes into one sample forsequencing. While single mRNA-sequence analysis is presently described,other types of nucleotides can be captured such as DNA and viruses froma cell or any molecular compound which can leverage phosphoramiditechemistry. Microfluidic devices can create tens of thousands ofprecisely sized (“monodisperse”) picoliter- or nanoliter-scale dropletsper minute (Thorsen et al., 2001; Umbanhowar, 2000). These droplets,which serve as tiny reaction chambers, have been used for PCR (Hindsonet al., 2011; Vogelstein and Kinzler, 1999), reverse transcription (Beeret al., 2008), cell viability screens (Brouzes et al., 2009), andfluorescence microscopy (Jarosz et al., 2014). However, a basicchallenge of using droplets for transcriptomics is to retain a molecularmemory of the identity of the cell from which each mRNA transcript wasisolated. The lack of effective molecular barcoding has prevented theapplication of droplets in many areas of genetics and genomics (Guo etal., 2012).

Here, Applicants address this challenge by introducing a barcodingsystem that endows each transcript with a droplet-specific moleculartag. Applicants' method, called Drop-Seq, combines droplet microfluidicswith massive molecular barcoding to simultaneously label and process themRNA transcripts from thousands of cells in one reaction for sequencing,without requiring mechanical sorting or picking of individual cells.

To demonstrate Drop-Seq's power to categorize cells in complex tissues,Applicants applied it to mouse retina. The retina is a powerful modelfor analysis of neural structure, function and development because,although it is about as complicated as any other part of the brain, itprovides a complete and accessible circuit in a compact volume (Hoon etal., 2014; Masland, 2012; Masland and Sanes, 2015; Sanes and Zipursky,2010). The retina contains five neuronal classes that are divided into˜100 types, only a minority of which have been molecularlycharacterized. Applicants used Drop-Seq to analyze 44,808 single cellsfrom the mouse retina, from which Applicants computationally assembledan ab initio cell classification of 39 cell types based solely onpatterns among the transcriptional profiles of many individual cells.This classification reproduces—in a single experiment—discoveries fromdecades of molecular, physiological, and anatomical investigations ofthe retina, while nominating many novel putative subtypes and specificmarkers. The results suggest how large-scale single-cell analysis willdeepen Applicants' understanding of the biology of complex tissues andcell populations.

To further demonstrate Drop-Seq's capability and capacity to categorizecells in complex tissues, Applicants applied Drop-Seq in human bonemarrow cells. Applicants explored human bone marrow cellular complexityon a limited number of cells and confirmed known key classificationsbased solely on their profiles.

Results

To efficiently profile vast numbers of individual cells, Applicantsdeveloped Drop-Seq, in which Applicants encapsulate cells in tinydroplets and barcode the transcripts from each individual droplet(encapsulated cell) to remember their cell of origin. Drop-Seq consistsof the following steps (FIG. 7A): (1) prepare a single-cell suspensionfrom a tissue; (2) co-encapsulate each individual cell with onedistinctly barcoded microparticle, bead or particle (e.g., microbead,macrobead, nanoparticle, etc.) in a nanoliter-scale droplet; (3) lysecells only after they have been isolated in droplets; (4) capture acell's mRNAs on its companion microparticle, forming STAMPs (Single-cellTranscriptomes Attached to Microparticles); (5) reverse-transcribe,amplify, and sequence thousands of STAMPs in a single reaction; and (6)use the STAMP barcodes to infer each transcript's cell of origin.Applicants describe the key components of this approach and theirvalidation.

A split-pool synthesis approach to generating large numbers ofdistinctly barcoded beads. The split-and-pool can occur after eachcycle, or after any specified number of cycles. Thus, each barcode ofinformation can range from a single nucleotide, to a dinucleotide ortrinucleotide, etc.

To deliver large numbers of barcoded primer molecules into individualdroplets, Applicants synthesized oligonucleotides directly on beads. Asa bead material, Applicants used a methacrylate resin, originallydeveloped for chromatography (Extended Experimental Procedures),composed of porous microparticles with substantial surface area. Avariety of bead materials are envisioned as useful bead substrates.Examples of bead materials which may be employed include any bead whichcan leverage phosphoramidate chemistry such as those used inoligonucleotide synthesis known to those skilled in the art. Specificexamples include, but are not limited to, functionalized polymers (e.g.,methylacrylates, polysterenes, polyacrylamides, polyethylenglycols),paramagnetic beads, and magnetic beads.

Applicants then used reverse-direction phosphoramidite synthesis tobuild oligonucleotides outwards from the microparticles from 5′ to 3′,yielding free 3′ ends available for enzymatic priming (Cheong et al.,2012; Kadonaga, 1991; Srivastava et al., 2008). Phosphoramiditesynthesis which is used to generate the barcodes, enables the chemicalmodification of any base along the oligonucleotide which can leveragethis type of chemistry. Specific examples include, but are not limitedto, barcoding with DNA bases, RNA bases, LNA bases, biotin-modifiedbases, fluorophore-conjugated bases, and non-canonical bases (i.e.,iso-G, iso-C, iso-A, etc.). Additionally, these barcoded beads can becombined with other forms of barcoding, such as optioal barcoding bypatterning the bead or fluorescent labelling with various fluorophoresor combinations of fluorophores.

Each microparticle-bound oligonucleotide is composed of five parts (FIG.7B): (1) a constant sequence (identical on all primers) for use as apriming site for PCR and sequencing; (2) a “cell barcode” that is thesame across all the primers on the surface of any one bead, butdifferent from the cell barcodes on all other beads; (3) a UniqueMolecular Identifier (UMI), different on each primer, that enablessequence reads derived from the same original mRNA molecule(amplification and PCR duplicates) to be identified computationally sothat they are not double-counted (Kivioja et al., 2012); (4) an oligo dTsequence (30 bases) (SEQ ID NO:1) for capturing polyadenylated mRNAs andpriming reverse transcription, and (5) a non-cleavable linker attachedto the surface of the bead material (not labelled) and the primingsequence.

To efficiently generate massive numbers of beads, each with millions ofcopies of a cell barcode distinct from the barcodes on the other beads,Applicants developed a “split-and-pool” synthesis strategy (FIG. 7C). Apool of millions of microparticles is divided into four equally sizedgroups; a different DNA base (A, G, C, or T) is added to each of thefour groups. The four groups of microparticles are then re-pooled,mixed, and re-split at random into another four groups, and another DNAbase (A, G, C, or T) is added to each of the four new groups. Afterrepeating this split-pool process 12 times, each bead's barcode reflectsthat bead's unique path through twelve synthesis reactions (FIG. 7C),such that all primers on a single microparticle possess the same one of4¹²=16,777,216 possible 12-bp barcodes. The entire microparticle poolthen undergoes eight rounds of degenerate oligonucleotide synthesis togenerate the UMI on each oligo (FIG. 7D); finally, an oligo dT sequence(T30) (SEQ ID NO:1) is synthesized on 3′ the end of all oligos on allbeads.

In various embodiments of oligonucleotide bound bead synthesis, optional“floppy bases” may be used, such as oligo dT which is presentlydescribed. However, these “floppy bases” are not limited to T-bases andany suitable base can be used anywhere from 0 to 20 bases.

While microbeads are presently described, this method is not limited to“micro” sized beads and any appropopriately sized bead is useful in anapplication where primers, PCR templates, transposons, siRNAs, orcapture probes are delivered to a target compartment. The bead cansimultaneously deliver both oligonucleotides and other chemicalcompounds, biological particles, or even reagents. Examples include butare not limited to a small molecule library, siRNA, an antibody, avirus, a bacterium, and so on. Thus, the bead size is related to theapplication of the bead. For example, a bead which is 1 cm in diametercan accommodate millions of primers then deliver the primers to a96-well titer plate, where then the linker is cleaved to release anddeliver the primers to these wells. Cleavable linkers can include avariety of polymers (or other types of “flexible” strain-chain compound)which hydrolyze under aqueous acidic or basic conditions, undergophotolysis, cleave under hydrogenation, or any method known to one ofskill in the art to release the bead from the mRNA or nucleotidesequence.

Applicants assessed the quality and complexity of Applicants' barcodedbeads in several ways. First, to estimate the number of primers permicroparticle, Applicants hybridized synthetic polyadenylated RNA tomicroparticles, eluted the synthetic RNA, and measured itsconcentration; from these experiments, Applicants estimate that eachbead contains more than 10⁸ primer sites (Extended ExperimentalProcedures). Second, to determine the ability to distinguish RNA basedon attached barcodes, Applicants reverse-transcribed synthetic RNAhybridized to 11 microparticles, amplified these barcoded cDNAs in asingle solution, and created a sequencing library (Extended ExperimentalProcedures). In the resulting sequence data, 11 cell barcodes eachconstituted 3.5%-14% of the sequencing reads, whereas the next mostabundant 12-mer at the barcode position constituted only 0.06% of reads(FIG. 13A). These results suggested that the microparticle-of-origin formost cDNAs can be recognized by sequencing. Finally, to assess thebarcode complexity, Applicants sequenced cell barcodes from 1,000microparticles and measured base and dinucleotide composition (FIG.13B), along with the number of unique cell barcodes that remained as thesequence was computationally truncated (FIG. 13C). All three analysessuggested that the sequence diversity of the cell barcodes approachedtheoretical limits, and therefore that the cell barcodes could easilydiscriminate among thousands of STAMPs.

Microfluidics device for co-encapsulating cells with beads. Applicantsdesigned a microfluidic “co-flow” device (Utada et al., 2007) toco-encapsulate cells with barcoded microparticles (FIGS. 8A, 14A). Thisdevice can quickly co-flow two aqueous solutions across an oil channelto form more than 50,000 nanoliter-sized droplets per minute. One flowcontains the barcoded microparticles, suspended in a lysis buffer; theother flow contains a cell suspension (FIG. 8A, left). Flow is laminarprior to encapsulation, so that the two solutions mix only after dropletformation. To maximize cell lysis and the diffusion of mRNAs onto thebead's surface, Applicants' device contains “mixers” in which rapidmixing by chaotic advection occurs in a bumpy, winding microfluidicchannel (Bringer et al., 2004).

The relative numbers of droplets, cells, and microparticles are key tothe efficacy of Drop-Seq. The number of droplets created greatly exceedsthe number of beads or cells injected, so that a droplet will generallycontain zero or one cells, and zero or one beads. Carefully selectingthe concentration of cells is also important for regulating cell-celldoublets and potential single-cell impurities, as Applicants discussbelow. Millions of nanoliter-sized droplets are generated per hour, ofwhich thousands contain both a bead and a cell. STAMPs are produced onlyin the subset of droplets that contain both a bead and a cell.

Sequencing and analysis of many STAMPs in a single reaction. Toefficiently analyze thousands of STAMPs at once, Applicants developed away to process the nucleic acids bound to any desired number ofmicroparticles in one reaction. Applicants first break the droplets in alarge volume of high-salt solution, to minimize the transfer of RNAsfrom bead to bead (Experimental Procedures). The mRNAs associated withthe microparticles are then reverse-transcribed together in onereaction, forming covalent STAMPs (FIG. 8A, step 7). (Reversetranscription can in principle be performed within the droplets, thoughApplicants found it to be more efficient outside the droplets,potentially due to cell lysate—derived factors that inhibit the reaction(White et al., 2011).) Critically, at this stage, a scientist can selectany desired number of STAMPs for analysis, much as one would select adesired number of cells from a cell suspension. STAMPs can be “banked”across multiple experiments; Applicants have stored STAMPs for more thantwo months without observing significant cDNA degradation (data notshown). Applicants PCR-amplify the barcoded cDNAs attached to STAMPs,then prepare 3′-end libraries by using a transposase to insert asequencing adapter into the cDNA (Experimental Procedures). Applicantssequence the resulting molecules from each end (FIG. 8C) usinghigh-capacity parallel sequencing (e.g., Illumina MiSeq, NextSeq, orHiSeq), and use these reads to assemble a matrix of digitalgene-expression measurements (counts of each gene in each cell) forfurther analysis (FIG. 8D, Experimental Procedures).

Drop-Seq has high single-cell specificity, as assessed in species-mixingexperiments. To determine whether Drop-Seq correctly remembers the cellfrom which individual transcripts were isolated, Applicants designedspecies-mixing experiments in which Applicants made suspensionscontaining cultured human (HEK) and mouse (3T3) cells. Nearly all humanor mouse mRNA sequence fragments can be unambiguously assigned to thecorrect genome of origin; a cell library's “organism purity” cantherefore be used to estimate its single-cell purity.

Applicants prepared Drop-Seq libraries from mixtures of human and mousecells, scoring the numbers of human and mouse transcripts thatassociated with each cell barcode in the sequencing data (FIG. 9A, 9B,14B). This analysis revealed that STAMPs associated to highlyorganism-specific sets of transcripts (FIGS. 9A and 9B), a result thatwould not be possible without high single-cell specificity. At deeplevels of sequencing that largely saturated sequencing of 82 STAMPs(737,240 reads per cell, FIG. 15) Applicants detected an average of44,295 transcripts from 6,722 genes in HEK cells, and 26,044 transcriptsfrom 5,663 genes in 3T3 cells (FIGS. 9C and 9D).

Single-cell purity of Drop-Seq libraries. It is important to understandthe limitations as well as the strengths of new technologies. Applicantstherefore characterized two sources of impurity in single-celllibraries.

Cell doublets. One mode of failure in any single-cell method involvescells that stick together or happen to otherwise be co-isolated forlibrary preparation. In some earlier methods, microscopy imaging ofwells has been used to identify “visible doublets” and establish a lowerbound on doublet rates. A previous study that used FACS to sort singlecells reported that 2.3% of wells contained visible cell doublets(Jaitin et al., 2014). The main commercial single-cell analysis platform(Fluidigm C1) images sets of 96 microfluidically isolated cells, in partso that users can identify doublets from these images; one recent studyidentified visible doublets in 11% ±9% of the capture chambers thatcontained cells (Shalek et al., 2014).

Molecular analysis by species mixing offers a powerful and sensitive newway to identify libraries prepared from doublets, and may identify manydoublets that are not detected by microscopy. For example, whenApplicants prepared species-mixed cell populations exactly as in theanalysis of Drop-Seq (FIGS. 9A, 9B) and analyzed them on the FluidigmC1, Applicants found 30% of the prepared libraries to be species-mixed(FIG. 14C) of which about one-third were visible doublets in themicroscopy images. When Applicants prepared Drop-Seq libraries from cellsuspensions at a cell concentration of 12.5 cells/μl (that allowsprocessing of about 1,200 cells per hour), almost all libraries werespecies-specific (FIG. 9A). When Applicants prepared Drop-Seq librariesfrom cell suspensions at a higher cell concentration (50 cells/μl),accommodating faster processing of cells (4,800 cells/hour), 1.9% of thesequenced STAMPs were species-mixed (FIG. 9B). Across four conditionsspanning 12.5 cells/μl to 100 cells/μl, there was a strong linearrelationship between the cell concentration used and the fraction ofspecies-mixed STAMPs (FIG. 15D; Experimental Procedures), reflecting thegreater chance that droplets encapsulate both a mouse and a human cellat higher cell concentrations. Since human-mouse doublets account forhalf of all cell-cell doublets, Applicants calculated overall doubletrates of 0.36% to 11.3% for the Drop-Seq conditions ranging fromhighest-purity to highest-throughput.

Single-cell impurity. A largely unexplored issue in single-cell analysisinvolves the extent to which single-cell libraries become contaminatedwith transcripts from other cells. The high throughput of Drop-Seq andApplicants' use of species-mixing experiments allowed us to carefullymeasure single-cell purity across thousands of single-cell librariesprepared at different cell concentrations. Applicants found thatimpurity was strongly related to the concentration at which cellsuspensions were loaded: organism purity ranged from 98.8% at 12.5cells/μl to 90.4% at 100 cells/μl (FIG. 15D). By mixing human and mousecell-to-library pipelines at different stages (cell suspension; dropletscontaining beads and lysed cells; post-droplet STAMPs), Applicants foundthat the cell suspension contributed 48% of impurities, RNA transferafter droplet breakage contributed 40%, and PCR artifacts contributed12% (FIG. 15E). Thus, the largest source of contamination appears to beambient RNA that is present in the cell suspension at the beginning ofthe experiment and presumably results from cells that are damaged duringpreparation. This result is important for single-cell transcriptomicsstudies, as the creation of cell suspensions is an indispensable firststep of almost all such methods. Indeed, when Applicants analyzed thesame species-mixed cell populations on a commercial single-cellsequencing platform (Fluidigm C1), Applicants measured a meansingle-cell purity of 95.8% (FIG. 15C), similar to Drop-Seq at 50cells/μl. It will be important to carefully evaluate all single-cellmethods using the kinds of species-mixing experiments performed here.

While the high-purity modes of Drop-Seq (FIG. 9A) would seem preferableto the highest-throughput modes (FIG. 9B) on these grounds, Applicantsnote that in may experimental contexts it may be desirable to processliving cells as quickly as possible, because ultra-fast processing ofliving cells may strengthen reproducibility and thereby help to realizea potential strength of Drop-Seq relative to slower-throughput, existingmethods. Applicants further explore these questions in the retinaexperiments below.

Drop-Seq samples about 12% of the transcripts in a cell. Applicants nextsought to understand how the digital single-cell transcriptomesascertained by Drop-Seq relate to the underlying mRNA content of cells.

Drop-Seq involves hybridization of RNAs to beads, which might affectmeasurements of genes' absolute expression levels, so Applicantscompared Drop-Seq expression measurements to those from a commonly usedin-solution cDNA amplification process, template switch amplification(Extended Experimental Procedures). While template switch amplificationis presently described, T7 linear amplification or exponentialisothermal amplification can also be used to amplify the product.Gene-level log-expression measurements in the two libraries were highlycorrelated (r=0.94, FIG. 9E), though Drop-Seq showed quantitativelylower ascertainment of GC-rich transcripts (FIG. 17A). Applicants alsocompared Drop-Seq single-cell log-expression measurements withmeasurements from bulk mRNA-seq, and observed a correlation of r=0.90(FIG. 9F).

An important and longstanding challenge in single-cell transcriptomicsis to understand how the RNAs ascertained in an experiment relate to theoriginal RNA contents of the cells. The increasing use of External RNAControls Consortium (ERCC) “spike-in” controls at known concentrations,together with UMIs to avoid double-counting, now allows estimation ofcapture rates for digital single-cell expression technologies (Brenneckeet al., 2013). Three recent studies estimated capture rates of currentsingle-cell digital-expression technologies at 3% (MARS-Seq) (Jaitin etal., 2014), 3.4% (CEL-Seq) (Grun et al., 2014), and 48% (5′-endSMART-seq) (Islam et al., 2014). Estimation of Drop-Seq capture ratesusing the correction method of Islam et al. (to try to avoiddouble-counting UMIs due to PCR or sequencing errors), generated acapture-rate estimate of 47% for Drop-Seq; however, Applicantsidentified evidence that sequencing errors can still inflate UMI counts,even when that correction method is used (Extended ExperimentalProcedures), so Applicants utilized the 8 bp UMI in Drop-Seq to derive amore conservative estimate (12.8%, FIG. 9G) based on a novel approach ofcollapsing similar UMI sequences into a single count. To furtherevaluate capture rates, Applicants made independent digital expressionmeasurements (on bulk RNA from 50,000 HEK cells) on 10 genes usingdroplet digital PCR (ddPCR) (Hindson et al., 2011). Drop-Seq captured onaverage 10.7% of the number of RNAs predicted by digital PCR (FIGS. 17D,17E, and 17F). These data indicate that the sensitivity of Drop-Seq iswithin the range established by recently developed digital expressionmethods, even when Applicants' novel and extremely conservative UMIcounting method is used to evaluate Drop-Seq.

Single-cell analysis of the cell cycle reveals continuously varying cellstates. To evaluate the visibility of cell states by Drop-Seq,Applicants first examined cell-to-cell variation among the 589 HEK and412 3T3 cells for which Applicants had prepared STAMPs in the aboveexperiment (61,697 reads per cell). Both cultures consist ofasynchronously dividing cells; principal components analysis (PCA) ofthe single-cell expression profiles showed the top components to bedominated by genes with roles in protein synthesis, growth, DNAreplication, and other aspects of the cell cycle (Table 5). Applicantsinferred the cell-cycle phase of each of the 1,001 cells by scoring forgene sets (signatures) reflecting five phases of the cell cyclepreviously characterized in chemically synchronized cells (G1/S, S,G2/M, M, and M/G1) (Table 6) (Whitfield et al., 2002). Genes in eachsignature co-varied across individual cells, allowing us to temporallyorder the cells along the cell cycle (FIG. 10A). Using this ordering,Applicants identified genes with expression patterns that vary along thecell cycle (at a false discovery rate of 5%; Experimental Procedures),yielding 544 and 668 genes in human (HEK) and mouse (3T3) cells,respectively (FIG. 10B). Most of the genes had peak expression in eitherthe G1+S or in the G2+M phases (FIG. 10B), with a minority displayingother patterns, such as peak expression at the M/G1 transition (e.g.cluster 8 in mouse cells, FIG. 10B). Among these genes, there was asignificant overlap in orthologous genes between the two species (200shared orthologs, P<10⁻⁶⁵ by hypergeometric test), consistent with aconserved cell cycle program. Most (82.5%) of these “conserved” cyclinggenes (the genes identified as cell cycle regulated in both species)have been previously annotated as related to the cell cycle in at leastone species. Among the 17.5% of conserved cycling genes that were notpreviously annotated as cell-cycle-regulated, Applicants found some thatwould be expected to show cell cycle variation (e.g. E2F7, NCAPG, CDCA4,DNMT1 and PARPBP), as well as some that to Applicants' knowledge werenot previously connected to the cell cycle, including transcriptionfactors (TCF19, ATF4, ZFHX4) and other genes (FIG. 10C).

Finally, Applicants found that in each species, four of the five top PCswere highly correlated with at least one of the cell cyclephase-specific scores (P<10⁻¹⁰, indicating a dominant role of the cellcycle in cell-to-cell variation in these cells, consistent with otherreports in dividing cells (Buettner et al., 2015). Thus, Drop-Seqsingle-cell profiles can uncover sets of genes that vary according tosubpopulation phenotypes. In particular, this enables study of the cellcycle without chemical synchronization and at high temporal resolutionacross a large number of cells, which may have assisted in identifyingconserved human-mouse gene pairs not previously known to oscillate withthe cell cycle.

Drop-Seq analysis of the retina reveals cell classes. Applicantsselected the retina to study with Drop-Seq because work over manydecades has generated information about many retinal cell types(Masland, 2012; Sanes and Zipursky, 2010), providing an opportunity torelate Applicants' single-cell RNA-seq data to existing cellclassification schemes. The retina contains five classes of neuronalcells, each defined by a combination of morphologic, physiologic, andmolecular criteria (FIG. 11A). The outermost of three cellular layerscontains photoreceptors, which transduce light into electrical signals.The middle layer contains three classes of interneurons—horizontal,bipolar and amacrine cells—as well as Müller glial cells. The innermostlayer contains retinal ganglion cells and some amacrine cells.Photoreceptors synapse onto interneurons, which process visual signalsand pass them to retinal ganglion cells, which in turn send them to therest of the brain. Most of the classes are divisible into discretetypes—a total currently estimated at about 100—but well under halfpossess molecular markers that distinguish them specifically from other,related types. Drop-Seq provides an opportunity to identify molecularsignatures of cell types previously defined exclusively by morphologicalor physiological criteria.

The retina presents formidable technical challenges for large-scalesingle cell profiling. First, about 70% of the cells in the retina arerod photoreceptors; the other retinal cell classes each comprise 0.5-8%of retinal cells and are further divided into types. The problem in theretina is therefore to identify a large number of individually rare celltypes. Second, the size variation among retinal cells—ranging from 1.2microns (rods) to 20 microns (retinal ganglion cells) in diameter andthus spanning three orders of magnitude in volume—can pose not onlytechnical challenges for unbiased isolation of cells, but alsocomplicate analysis because of huge cell-to-cell differences in mRNAcontent.

Applicants performed Drop-Seq on cell suspensions made from wholeretinas of 14-day-old mice, sequencing 49,300 STAMPs to an average depthof 14,084 reads (STAMPs were collected in seven experimental batchesover four days). To discover cell types from single-cell expressionprofiles ab initio, Applicants first performed principal componentsanalysis, using the genes that showed a greater degree of expressionvariance (across cells) than could be explained by random statisticalsampling of the transcripts (within cells), and initially focusing onthe 13,155 cells with the largest numbers of transcripts, to reduce theotherwise-disproportionate contribution of tiny photoreceptor cells tothe analysis (Experimental Procedures). Applicants utilized a classicpermutation test (Peres-Neto et al., 2005) and a recently developedresampling procedure (Chung and Storey, 2014) to identify statisticallysignificant principal components (PCs), finding 32 significant PCs inthese data (FIG. 18). Almost all of the significant PCs were stronglyshaped by genes that are well-known markers of retinal cell types.Applicants used the cell loadings associated with these principalcomponents as input for t-Distributed Stochastic Neighbor Embedding(tSNE) (van der Maaten and Hinton, 2008), to reduce these 32 PCs to twodimensions. Applicants projected the remaining 36,145 cells in the dataonto the tSNE, and combined a density clustering approach withdifferential expression analysis to identify distinct clusters of cellsfrom this tSNE analysis (Extended Experimental Procedures). These stepsleft us with 39 transcriptionally distinct cell populations—the largestcontaining 29,400 cells, the smallest containing 50 cells, altogethercomposed of 44,808 cells (FIG. 11B). Finally, Applicants organized the39 cell populations into larger categories (classes) oftranscriptionally similar clusters, by building a dendrogram ofsimilarity relationships among the 39 cell populations based upon theirEuclidean distances in gene-expression space (FIG. 11D, left).

Applicants found that their unsupervised clustering results—which werederived entirely from clustering the single-cell transcriptome dataitself, rather than being “instructed” by known markers—correlatedstrikingly with expression of the known molecular markers that exist formany retinal cell types (FIG. 11D, right). Well-known markers of retinalcell types include Slc17a6 (Vglut2) and Thy1 for retinal ganglion cells,Vsx2 for bipolar cells, Lhx1for horizontal cells, opsins forphotoreceptors, Tfap2b and Pax6 for amacrine cells, and Rlbp1 for Mullerglia. Each of these markers showed single-cell patterns of geneexpression that corresponded to a branch or leaf of the dendrogramderived from Applicants' unsupervised analysis (FIG. 11D).Photoreceptors clustered into two groups that were readily identifiableas rods and cones based on their expression of rod and cone opsins.Additional clusters corresponded to non-neural cells associated withretina, including astrocytes (associated with retinal ganglion cellaxons exiting the retina), resident microglia (Provis et al., 1996),endothelial cells (from intra-retinal vasculature), pericytes (cellsthat surround the endothelium), and fibroblasts (FIG. 11D). Furthermore,Applicants found that the relative proportions of the major cell classesin Applicants' data largely agreed with earlier estimates frommicroscopy (Jeon et al., 1998). The ability of an unsupervised analysisto identify all of these biologically known cell classes at the expectedratios suggests that such analyses may be applicable to many othertissues whose resident cell populations are far less characterized.

Replication and cumulative power of Drop-Seq data. Replication acrossexperimental sessions enables the construction of cumulatively morepowerful datasets for detection of subtle biological signals. Theretinal STAMPs were generated on four different days (weeks apart),utilizing four different mouse litters, with several sessions generatingmultiple replicate Drop-Seq runs, for a total of seven replicates.Applicants prepared one of these replicates at a particularly low cellconcentration (15 cells/μl) and high purity, to evaluate whether anyanalytical results were artifacts of cell-cell doublets or single-cellimpurity (i.e. whether they excluded these “high-purity” cells), asDrop-Seq's fastest-throughput modes allow extremely fast processing ofliving cells (valuable for maintaining correspondence to the in vivosystem) but at some cost in single-cell purity relative to itshighest-purity modes (FIG. 9A, 9B), and the correspondence betweentranscriptional patterns identified in these modes was important tounderstand. A key question, then, was whether every experimental sessioncontributed cells to each of the 39 populations that Applicants hadobserved in the above analysis (FIG. 11B). Applicants found that all 39clusters contained cells from every experimental session and condition.However, Cluster 36 (arrow in FIG. 11E; star in FIG. 20), drewdisproportionately from replicates two and three. This cluster expressesmarkers of fibroblasts, a cell type that is not native to the retina butis instead present in tissue surrounding the retina; the inclusion oflarger numbers of fibroblasts in two replicates most likely representsthe challenge of dissecting around the retinal perimeter. Mostimportantly, the 3,226 cells prepared under high-purity conditions(replicate 7) contributed to every cluster, indicating that none of theclusters is an artifact of doublets or other impurities (FIG. 11E).While Applicants cannot exclude the possibility that experimentalvariation influences gene expression measurements in Drop-Seq, in theseexperiments such effects appeared to be small relative to thedifferences even between highly similar cell subtypes (e.g. the 21populations of amacrines cells described below).

Applicants next examined how the classification of cells (based on theirpatterns of gene expression) evolved as a function of the numbers ofcells in analysis, in order to evaluate both the robustness of theclustering analysis and the scientific return to analyzing large numbersof cells. Applicants used 500, 2,000, or 9,431 cells from Applicants'dataset, and asked how (for example) amacrine cells identified in thefull (44,808-cell analysis) had clustered in analyses of smaller numbersof cells (FIG. 11F). Applicants found that as the number of cells in thedata increased, distinctions between related clusters become clearer,stronger, and finer in resolution, with the result that a greater numberof rare amacrine cell populations (each representing 0.1-0.9% of thecells in the experiment) could ultimately be distinguished from oneanother (FIG. 11F). In analyses of smaller numbers of cells, these cellswere often co-clustered into “supertypes”, reflecting the challenge ofdistinguishing recurring patterns (often involving small numbers ofgenes) from single-cell biological, technical, and statistical noise ingenome-wide experiments.

Profiles of 21 candidate amacrine cell types. To better understand theability of single-cell analysis to distinguish between closely relatedcell types, Applicants focused on the 21 clusters identified as amacrineneurons, the neuronal class considered to be the most morphologicallydiverse (Masland, 2012). Most amacrine cells are inhibitory, with aroundhalf using glycine and the other half using GABA as a neurotransmitter..Excitatory amacrine cells, expressing Slc17a8 (VGlut3) and releasingglutamate, have also been identified (Haverkamp and Wassle, 2004).Another recently discovered amacrine cell population release no knownclassical neurotransmitter (nGnG amacrines) (Kay et al., 2011).

Applicants first identified potential amacrine markers that were themost universally expressed by amacrine clusters relative to other cellclasses (FIG. 12A). Applicants then assessed the expression of knownglycinergic and GABAergic markers; their mutually exclusive expressionis seen as a fundamental distinction with a morphological correlate:most GABAergic amacrines have broad dendritic arbors restricted to asingle sublamina (wide-field) whereas glycinergic amacrines have narrowdendritic arbors that span multiple sublaminae (narrow-field). Of the 21clusters of amacrine cells, 12 groups (together comprising 2,516 cells)were identifiable as GABAergic and a distinct 5 clusters (togethercomprising 1,121 cells) as glycinergic, based on expression of the GABAsynthetic enzyme, glutamate decarboxylase (two isoforms, encoded by Gad1and Gad2) and the glycine transporter (S1c6a9), respectively (FIG. 12B).An additional cell population (comprising 73 cells) was identified asexcitatory by its expression of Slc17a8, which was not expressed inother amacrine populations (FIG. 12B). The remaining three amacrine cellpopulations (clusters 4, 20, and 21) had absent or low levels of Gad1,Gad2, Slc6a9, and Slc17a8; these likely include nGnG amacrines, asdescribed below.

The amacrine types with known molecular markers were readily assigned tospecific cell populations (clusters) from the analysis. Glycinergic A-IIamacrine neurons appeared to correspond to the most divergentglycinergic cluster (FIG. 12B, cluster 16), as this was the only clusterto strongly express the Gjd2 gene encoding the gap junction proteinconnexin 36 (Feigenspan et al., 2001; Mills et al., 2001). Ebf3, atranscription factor found in SEG glycinergic as well as nGnG amacrines,was specific to clusters 17 and 20. Starburst amacrine neurons (SACs),the only retinal cells that use acetylcholine as a co-transmitter, wereidentifiable as cluster 3 by those cells' expression of the cholineacetyltransferase gene Chat (FIG. 12B); the Drop-Seq data also suggestedthat SACs, unlike the other GABAergic cells, expressed Gadl but notGad2, as previously observed in rabbit (Famiglietti and Sundquist,2010).

Beyond the above distinctions, little is known about moleculardistinctions among the physiologically and morphologically diverseamacrine types. Molecular markers of these types would be powerful toolsfor more comprehensively studying amacrines' circuitry, development, andfunction. For each of the 21 amacrine cell populations (clusters),Applicants identified multiple genes that were highly enriched in eachcluster relative to the other amacrines (FIG. 12C). Many markers of eachcluster (FIG. 12C) are genes involved in neurotransmission orneuromodulation; such genes have historically been good markers ofindividual neuronal cell types in other brain regions.

Can Drop-Seq identify novel markers of cell types? Applicants analyzedgenes expressed in two of the amacrine clusters: cluster 7, a GABAergiccluster, and cluster 20, which had a mixture of glycinergic and nGnGcells. First, Applicants co-stained retinal sections with antibodies tothe transcription factor MAF, the top marker of cluster 7, plusantibodies to either GAD1 or SLC6A9, markers of GABAergic andglycinergic transmission, respectively. As predicted by Drop-Seq data,MAF was found specifically in a small subset of amacrine cells that wereGABAergic and not glycinergic (FIG. 12D). Cluster 7 had numerous genesthat were enriched relative to its nearest neighbor, cluster 6 (FIG.12E, 16 genes>2.8-fold enrichment, p<10⁻⁹), including Crybb3, whichbelongs to the crystallin family of proteins that are known to bedirectly upregulated by Maf during ocular lens development (Yang andCvekl, 2005), and another, the matrix metalloproteinase Mmp9, that hasbeen shown to accept crystallins as a substrate (Descamps et al., 2005;Starckx et al., 2003). Second, Applicants stained sections withantibodies to PPP1R17, which was selectively expressed in cluster 20.Cluster 20 shows weak, infrequent glycine transporter expression and isone of only two clusters (with cluster 21) that express Neurod6, amarker of nGnG neurons (Kay et al., 2011), which are neither glycinergicnor GABAergic. Applicants used a transgenic strain (MitoP) that has beenshown to express cyan fluorescent protein (CFP) specifically in nGnGamacrines (Kay et al., 2011). PPP1R17 stained in 85% of all CFP-positiveamacrines in the MitoP line, validating this as a marker of nGnG cells.The absence of PPP1R17 from putative nGnG amacrines in Cluster 21suggests a hitherto unsuspected level of heterogeneity among nGnGamacrines. Like cluster 7, cluster 20 expressed numerous markersdistinguishing it from its closest neighbor (FIG. 12G; 12 genes>2.8-foldenrichment, p<10⁻⁹).

Identification of additional cellular diversity within individualclusters. Applicants' unsupervised clustering analysis grouped cellsinto 39 distinct populations; as many as 100 retinal cell types areproposed to exist based on morphology or physiology. Applicantstherefore asked whether additional heterogeneity and populationstructure might exist within clusters and be visible in supervisedanalyses; this would suggest that still-deeper classification willbecome possible with larger numbers of cells, or with combinations ofunsupervised and known-marker-driven analyses. Here Applicants focus oncone photoreceptors and retinal ganglion cells.

Cones. Mice are dichromats, having only short-wavelength (blue or S-)and middle-wavelength (green or M-) opsins, encoded by the genes Opn1swand Opn1mw, respectively. The S- and M-opsins are expressed in opposinggradients along the dorsal-ventral axis, with many cones, especially incentral retina, expressing both of these opsins (Szel et al., 2000). Noother genes have been identified that selectively mark S- or M-cones.

Applicants identified cluster 25 as cones by their expression of Opn1mw,Opn1sw, Arr3, and other cone-specific genes. Applicants comparedgenome-wide gene expression in 336 cells (in cluster 25) expressing onlyOpn1sw (the blue-light-sensitive opsin) to expression in 551 cells (inthe same cluster) expressing only Opn1mw (the green-light-sensitiveopsin) (FIG. 1211). Eight genes differed in expression by at least2-fold (and at p<10⁻⁹) between the two cell populations. One such gene,Thrb, encodes the receptor for thyroid hormone, a key developmentalregulator of the dorsal-ventral patterning that shapes differentialopsin expression (Roberts et al., 2006). Two other genes, Smug1 andCcdc136, have been shown to be concentrated in dorsal and ventral conesrespectively (Corbo et al., 2007), consistent with Applicants'assignment of them to M- and S-cones.

Retinal ganglion cells. Retinal ganglion cells (RGCs), the sole outputneuron class from the retina, are believed to consist of about 20 types,of which several have known molecular markers (Masland and Sanes, 2015).RGCs altogether comprise less than 1% of the cells in the retina (Jeonet al., 1998). In Applicants' analysis of 44,808 cells, Applicantsidentified a single RGC cluster, consisting of less than 1% of all cellsanalyzed. Opn4, the gene encoding melanopsin, is a known marker of adistinct RGC type (Hattar et al., 2002); among the 432 RGCs, Applicantsidentified 26 cells expressing Opn4. These 26 cells expressed sevengenes at least two-fold more strongly than the 406 Opn4- RGCs did(p<10⁹, FIG. 12I); one of these seven genes was Eomes, recently shown tobe required for development and maintenance of melanopsin-containingRGCs (Mao et al., 2014).

Human bone marrow cells. Human bone marrow cells contain multipotenthaematopoietic stem cells which differentiate into two types ofprogenitors: lymphoid stem cells and myeloid stem cells. Lymphoid stemcells differentiate to prolymphocytes which develop into T, B and NKcells (i.e., peripheral blood monocuclear cells), while myeloid stemcells differentiate into three types of cell lines: granulocyte-monocyteprogentiors, erythroid progenitors, and megakaryocytes. Peripheral bloodmonoclear cells (PBMCs) consist of blood cells with a round nucleuswhich are involved in fighting diseases such as leukemais, cancers, andinfectious diseases. Applicants' analysis of 471 single-celltranscription profiles prepared by Drop-Seq identified 8 clusters ofgene markers which correlated to known cell types of haematopoietic stemcells.

Discussion

Here Applicants have described Drop-Seq, a new technology forsimultaneously analyzing genome-wide expression in unconstrained numbersof individual cells. Applicants first validated Drop-Seq by profilingmixtures of intact human and mouse cells. Applicants then used Drop-Seqto ascertain cell states in a nominally homogeneous cell population andcell types in a complex tissue. To analyze cell states, Applicantsprofiled the cell cycle at near-continuous temporal resolution across1,001 asynchronously growing cells from two species, uncovering novelcell cycle-regulated genes with evolutionarily conserved expressionoscillations. To analyze cell types, Applicants profiled 44,808individual cells from the mouse retina, an accessible portion of thecentral nervous system. Applicants identified 39 transcriptionallydistinct cell populations in the retina, revealed novel relationshipsamong those cells, and nominated new cell type-specific markers, two ofwhich Applicants validated by immunohistochemistry.

In other embodiments of the technology, the application of thetechnology can be used to identify novel biomarkers of a disease, suchas cancer or an autoimmune disease, by identifying cell populations,cell markers, or combinations of cell populations, that are specificallypresent in a disease state versus a healthy state.

In a further application, the Drop-Seq technology can be applied todisease modeling or prognosticating disease. The single-cell techniquecan be utilized to diagnose diesases with unclear etiologies or origins.For example, cancer of unknown primary tissue could be traced to atissue-of-origin by identifying rare cells in the tissue that expressmarkers of a cell-type of a particular tissue.

As discussed above, the Dropq-Seq process generates STAMPs (single-celltranscriptomes attached to microparticles). Hence, the microparticle hasa stable record of the mRNAs present in a cell and therefore can beprobed for expression of different genes. Fo example, since the Drop-Seqtechnology can be utilized to rapidly sequence genes in parallel, itwould be possible to probe those genes associated with a phenotypedifference in microbiomes associated with human bodies. The technologycan therefore be extended to analyze molecules, organelles, cellularfragments (e.g., synapses), whole cells, or collection of cells (i.e.,organoids).

To become widely adopted, and to advance biology, a new technologyshould possess these characteristics:

1. It should fill an unmet scientific need. Biologists are quicklyrecognizing the scientific opportunities enabled by ascertainingtranscriptional variation at the cellular level. Current methods,however, can profile only up to a few hundred cells per day, at a costof $3-$50 per cell. By contrast, a single scientist employing Drop-Seqcan completely prepare 10,000 single-cell libraries for sequencing, forabout 6 cents per cell. Applicants hope that ease, speed, and low costfacilitate exuberant experimentation, careful replication, and manycycles of experiments, analyses, ideas, and more experiments.

2. It should be easy to adopt. The simpler a technology, the greater thelikelihood that it can be adopted by the scientists who will know how toput it to good use. Drop-Seq utilizes equipment that is available to anybiology lab—a small inverted microscope and syringe pumps such as thoseroutinely used for microinjection. A Drop-Seq setup can be constructedquickly and inexpensively (FIG. 21 and Extended ExperimentalProcedures). Drop-Seq also uses two novel reagents: the microfluidicdevices for droplet preparation, and the beads to individually barcodeeach cell's RNA. Applicants designed the microfluidics devices (through30 design iterations) to be simple, passive devices that could bereadily constructed in any academic or commercial microfluidicsfacility, and Applicants provide a CAD file to enable this. The barcodedbeads described here will be available upon the publication of thispaper (Extended Experimental Procedures). Applicants' supplementalmaterials include detailed protocols for interested readers.

3. It should be thoroughly tested to provide a clear understanding ofthe technology's advantages and limitations. Here Applicants usedmixtures of mouse and human cells to carefully measure both single-cellpurity and the frequency of cell doublets—the first work that Applicantsare aware of to test any single-cell analysis strategy in this way.Applicants find that Applicants can tune two key qualityparameters—cell-cell doublets and contaminating RNA—by adjusting theinput cell concentration, and that at lower cell concentrations (stillaccommodating a throughput of 1,200 cells per hour) Drop-Seq comparesfavorably to existing technology for both doublets and purity.Applicants' results suggest that other methods of isolating single cellsfrom a cell suspension, such as fluorescence activated cell sorting(FACS) or microfluidics, are also vulnerable to doublets and single-cellimpurities. The analysis of Applicants' retina dataset suggests thateven relatively impure libraries generated in “ultra-high-throughput”modes (100 cells per μl, allowing the processing of 10,000 cells perhour at ˜10% doublet and impurity rates) can yield a rich, robust andbiologically validated cell classification, but other tissues orapplications may require using purer modes of Drop-Seq. Applicants wouldalways suggest that pilot analyses begin with one of Drop-Seq'shigher-purity modes.

The other major quality metric of a single-cell profiling technology iscapture efficiency. Applicants estimated Drop-Seq's capture efficiencyto be about 12%, based on analyses of synthetic RNA “spike-ins,” whichApplicants then corroborated by highly sensitive digital PCRmeasurements of ten genes. Studies of single-cell digital expressionprofiling methods in the past year have reported capture rates of 3%,3.4%, and 48%, though these rates have not been estimated or correctedin uniform ways; Applicants chose a particularly conservative estimationmethod to arrive at the 12% estimate for Drop-Seq and suggest that agreat need in single-cell genomics is for uniform comparison strategiesand metrics. Applicants' analysis of the retina indicates that capturingonly ˜12% of each cell's transcriptome (and sequencing less than that)may allow even subtle cell type differences (e.g. among 21 amacrine cellpopulations) to be recognized; this extends an idea proposed in a recentstudy of 301 cortical cells (Pollen et al., 2014). The ability toanalyze so many cells may help to elucidate biological patterns thatwould otherwise be elusive, as these patterns are then shared acrosslarge numbers of analyzed cells in ways that overwhelm the biological,technical and statistical-sampling noise that exists at the single-celllevel.

Unsupervised computational analysis of Drop-Seq data identified 39transcriptionally distinct retinal cell populations; all turned out tobelong to known cell classes, and most appeared to correspond to knownor hypothesized retinal cell types and subtypes, based on expression ofpreviously validated markers (FIGS. 11 and 12). It is a particularstrength of the retina that establishing correspondence between clusterand type was in many cases straightforward; classification has notproceeded sufficiently far in most other parts of the brain to permitsuch validation, which is why initial validation in a tissue like theretina was so important. Many of these cell populations—especially thosewithin the amacrine class—nominated new distinguishing markers for cellspreviously identified only by morphology and physiology.

Many interesting questions surround the definition of cell types fromtranscriptomics data. For example, are there always clear expressionthresholds beyond which two groups of cells are distinct types, or aredistinctions sometimes graded and continuous? More importantly, how dotranscriptional differences among cell populations give rise toanatomical and physiological differences? The throughput afforded byDrop-Seq may enable such questions to be comprehensively addressed inwhole tissues, by providing sufficient numbers of profiles to appreciatepatterns of expression even in rare cell types.

Applicants see many other important applications of Drop-Seq in biology,beyond the identification of cell types and cell states. Genome-scalegenetic studies are identifying large numbers of genes in which geneticvariation contributes to disease risk; but biology has lacked similarlyhigh-throughput ways of connecting genes to specific cell populationsand their unique functional responses. Finding the cellular sites andbiological activities of so many genes will be important for going fromgenetic leads to biological insights. High-throughput single-celltranscriptomics could localize the expression of risk genes to specificcell types, and in conjunction with genetic perturbations, could alsohelp to systematically relate each gene to (i) the cell types mostaffected by loss or perturbation of those genes; and (ii) thealterations in cell state elicited by such perturbations. Suchapproaches could help cross the daunting gap from high-throughput genediscovery to (harder-to-acquire) real insights about the etiology ofhuman diseases (McCarroll et al., 2014).

The coupling of Drop-Seq to additional perturbations—such as smallmolecules, mutations (natural or engineered), pathogens, or otherstimuli—could be used to generate an information-rich, multi-dimensionalreadout of the influence of perturbations on many kinds of cells. Whenstudying the effects of a mutation, for example, Drop-Seq couldsimultaneously reveal the ways in which the same mutation impacts manycell types in both cell-autonomous and cell-nonautonomous ways.

The functional implications of a gene's expression are a product notjust of the gene or encoded protein's intrinsic properties, but also ofthe entire cell-level context in which the gene is expressed. Applicantshope Drop-Seq will enable the abundant and routine discovery of suchrelationships in many areas of biology.

Experimental Procedures

Device fabrication. Microfluidic devices were designed using AutoCADsoftware (Autodesk, Inc.), and the components tested using COMSOLMultiphysics (COMSOL Inc.). A CAD file is also available in thesupplement.

Devices were fabricated using a bio-compatible, silicon-based polymer,polydimethylsiloxane (PDMS) via replica molding using the epoxy-basedphoto resist SU8 as the master, as previously described (Mazutis et al.,2013; McDonald et al., 2000). The PDMS devices were then renderedhydrophobic by flowing in Aquapel (Rider, Mass., USA) through thechannels, drying out the excess fluid by flowing in pressurized air, andbaking the device at 65° C. for 10 minutes.

Barcoded microparticle synthesis. Bead functionalization and reversedirection phosphoramidite synthesis were performed by Chemgenes Corp(Wilmington, Mass.). “Split-and-pool” cycles were accomplished byremoving the dry resin from each column, hand mixing, and weighing outfour equal portions before returning the resin for an additional cycleof synthesis. Full details (including availability of the beads) aredescribed in Extended Experimental Procedures.

Drop-Seq procedure. A complete, in-depth description of the protocol,including the composition and catalogue numbers for all reagents, can befound in Extended Experimental Procedures. In brief, droplets ˜1 nL insize were generated using the co-flow microfluidic device describedabove, in which barcoded microparticles, suspended in lysis buffer, wereflowed at a rate equal to that of a single-cell suspension, so that thedroplets were composed of an equal amount of each component. As soon asdroplet generation was complete, droplets were broken withperfluorooctanol in 30 mL of 6×SSC. The addition of a large aqueousvolume to the droplets reduces hybridization events after dropletbreakage, because DNA base pairing follows second-order kinetics(Britten and Kohne, 1968; Wetmur and Davidson, 1968). The beads werethen washed and resuspended in a reverse transcriptase mix. Afterincubation for 30 min at 25° C. and 90 min at 42° C., the beads werewashed and resuspended in Exonuclease I mix and incubated for 45 min at37° C. The beads were washed, counted, aliquoted into PCR tubes, and PCRamplified (see Extended Experimental Procedures for details). The PCRreactions were purified and pooled, and the amplified cDNA quantified ona BioAnalysis High Sensitivity Chip (Agilent). The 3′-ends werefragmented and amplified for sequencing using the Nextera XT DNA sampleprep kit (Illumina) using custom primers that enabled the specificamplification of only the 3′ ends (Table 9). The libraries were purifiedand quantitated on a High Sensitivity Chip, and sequenced on theIllumina NextSeq 500. All details regarding reaction conditions, primersused, and sequencing specifications can be found in the ExtendedExperimental Procedures.

Alignment and estimation of digital expression levels. Raw sequence datawas filtered, adapter- and polyA-trimmed, and aligned to either themouse (mm10) genome for retina experiments, or a combined mouse(mm10)—human (hg19) mega-reference, using STAR v2.4.0 (Dobin et al.,2013). All reads with the same cell barcode were grouped together, andreads from the same cell aligning to the same gene, with UMIs withinED=1, were merged. On each cell, for each gene, the unique UMIs werecounted; this count was then placed into a digital expression matrix.The matrix was ordered by the sum of all UMIs per cell, and a cumulativesum plot was generated. Applicants determined the number of STAMPs byestimating the first inflection point (FIG. 14B), which Applicantsempirically found to always be close to the estimated number ofamplified STAMPs. Additional details can be found in ExtendedExperimental Procedures.

Cell cycle analysis of HEK and 3T3 cells. Gene sets reflecting fivephases of the HeLa cell cycle (G1/S, S, G2/M, M and M/G1) were takenfrom Whitfield et al. (Whitfield et al., 2002), with some modification(Extended Experimental Procedures). A phase-specific score was generatedfor each cell, across all five phases, using averaged normalizedexpression levels (log₂(TPM+1)) of the genes in each gene set. Cellswere then ordered along the cell cycle by comparing the patterns ofthese five phase scores per cell. To identify cell cycle-regulatedgenes, Applicants used a sliding window approach, and identified windowsof maximal and minimal average expression, both for ordered cells, andfor shuffled cells, to evaluate the false-discovery rate. Full detailsmay be found in Extended Experimental Procedures.

Generation of whole retina suspension. Suspensions were prepared fromthe retinas of 14-day-old (P14) C57BL/6 mice by adapting previouslydescribed methods (Barres et al., 1988). See Extended ExperimentalProcedures for additional details.

Principal components and clustering analysis of retina data. Principalcomponents analysis (PCA) was first performed on a 13,155-cell “trainingset” of the 49,300-cell dataset, using single-cell libraries with >900genes. Applicants found their approach was more effective in discoveringstructures corresponding to rare cell types than performing PCA on thefull dataset, which was dominated by numerous, tiny rod photoreceptors(Extended Experimental Procedures). 384 genes that showed eithersignificant variability or structure within this training set were usedto learn the principal components (PCs). Thirty-two statisticallysignificant PCs were identified using a permutation test andindependently confirmed using a modified resampling procedure (Chung andStorey, 2014). To visualize the organization of cell-types in theretina, Applicants projected individual cells within the training setbased on their scores along the significant PCs onto a singletwo-dimensional map using t-Distributed Stochastic Neighbor Embedding(t-SNE) (van der Maaten and Hinton, 2008). The remaining 36,145single-cell libraries (<900 genes detected) were next projected on tothis t-SNE map, based on their representation within the PC-subspace ofthe training set (Berman et al., 2014; Shekhar et al., 2014). Thisapproach mitigates the impact of noisy variation in the lower complexitylibraries due to gene dropouts, and was also reliable in the sense thatwhen Applicants withheld from the tSNE all cells from a given clusterand then tried to project them, these withheld cells were not spuriouslyassigned to another cluster by the projection (Table 10). Furthermore,cells are not allowed to be projected based on similarity to less than10 cells (see Extended Experimental Procedures). Point clouds on thet-SNE map represent cell-types, and density clustering (Ester et al.,1996) identified these regions, using two sets of parameters fordefining both large and small clusters. Differential expression testing(McDavid et al., 2013) was then used to confirm that clusters weredistinct from each other. Hierarchical clustering based on Euclideandistance and complete linkage was used to build a tree relating theclusters. Applicants noted expression of several rod-specific genes,such as Rho and Nrl, in every cell cluster, an observation that has beenmade in another retinal cell gene expression study (Siegert et al.,2012). This likely arises from solubilization of these high-abundancetranscripts during cell suspension preparation. Additional informationregarding retinal cell data analysis can be found in the ExtendedExperimental Procedures.

Example 3 Extended Experimental Procedures for Example 2

Bead Synthesis. Bead functionalization and reverse directionphosphoramidite synthesis (5′ to 3′) were performed by Chemgenes Corp.Toyopearl HW-65S resin (30 micron mean particle diameter) was purchasedfrom Tosoh Biosciences, and surface alcohols were functionalized with aPEG derivative to generate an 18-carbon long, flexible-chain linker. Thefunctionalized bead was then used as a solid support for reversedirection phosphoramidite synthesis (5′→3′) on an Expedite 8909 DNA/RNAsynthesizer using DNA Synthesis at 10 micromole cycle scale and acoupling time of 3 minutes. Amidites used were:N⁶-Benzoyl-3′-O-DMT-2′-deoxyadenosine-5′-cyanoethyl-N,N-diisopropyl-phosphoramidite (dA-N⁶-Bz-CEP);N⁴-Acetyl-3′-O-DMT-2′-deoxy-cytidine-5′-cyanoethyl-N,N-diisopropyl-phosphoramidite(dC-N⁴-Ac-CEP); N²-DMF-3′-O-DMT-2′-deoxyguanosine-5′-cyanoethyl-N,N-diisopropyl-phosphoramidite (dG-N²-DMF-CEP);and 3′-O-DMT-2′-deoxythymidine-5′-cyanoethyl-N,N-diisopropyl-phosphoramidite (T-CEP). Aceticanhydride and N-methylimidazole were used in the capping step;ethylthio-tetrazole was used in the activation step; iodine was used inthe oxidation step, and dichloroacetic acid was used in the deblockingstep. After each of the twelve split-and-pool phosphoramidite synthesiscycles, beads were removed from the synthesis column, pooled,hand-mixed, and apportioned into four equal portions by mass; these beadaliquots were then placed in a separate synthesis column and reactedwith either dG, dC, dT, or dA phosphoramidite. This process was repeated12 times for a total of 4̂12=16,777,216 unique barcode sequences. Forcomplete details regarding the barcoded bead sequences used.

Cell Culture. Human 293 T cells were purchased as well as the murineNIH/3T3 cells. 293T and 3T3 cells were grown in DMEM supplemented with10% FBS and 1% penicillin-streptomycin.

Cells were grown to a confluence of 30-60% and treated with TrypLE forfive min, quenched with equal volume of growth medium, and spun down at300×g for 5 min. The supernatant was removed, and cells were resuspendedin 1 mL of 1× PBS +0.2% BSA and re-spun at 300×g for 3 min. Thesupernatant was again removed, and the cells re-suspended in 1 mL of 1×PBS, passed through a 40-micron cell strainer and counted. For Drop-Seq,cells were diluted to the final concentration in 1× PBS+200 μg/mL BSA.

Generation of Whole Retina Suspensions. Single cell suspensions wereprepared from P14 mouse retinas by adapting previously described methodsfor purifying retinal ganglion cells from rat retina (Barnes et al.,1988). Briefly, mouse retinas were digested in a papain solution (40 Upapain/1.0 mL DPBS) for 45 minutes. Papain was then neutralized in atrypsin inhibitor solution (0.15% ovomucoid in DPBS) and the tissue wastriturated to generate a single cell suspension. Following trituration,the cells were pelleted and resuspended and the cell suspension wasfiltered through a 20 μm Nitex mesh filter to eliminate any dumped cellsand this suspension was then used for Drop-Seq. The cells were thendiluted in DPBS+0.2% BSA to either 200 cells/μl (replicates 1-6) or 30cells/μl (replicate 7).

Retina suspensions were processed through Drop-Seq on four separatedays. One library was prepared on day 1 (replicate 1); two libraries onday 2 (replicates 2 and 3); three libraries on day 3 (replicates 4-6);and one library on day 4 (replicate 7, high purity). To replicates 4-6,human HEK cells were spiked in at a concentration of 1 cell/μl (0.5%)but the wide range of cell sizes in the retina data made it impossibleto calibrate single-cell purity or doublets using the cross-speciescomparison method. Each of the seven replicates was sequenced separately

Drop-Seq

Preparation of beads. Beads (either Barcoded Bead SeqA or Barcoded BeadSeqB; Table 9 and see note at end of Extended Experimental Procedures)were washed twice with 30 mL of 100% EtOH and twice with 30 mL of TE/TW(10 mM Tris pH 8.0, 1 mM EDTA, 0.01% Tween). The bead pellet wasresuspended in 10 mL TE/TW and passed through a 100 μm filter into a 50mL Falcon tube for long-term storage at 4° C. The stock concentration ofbeads (in beads/pL) was assessed using a Fuchs-Rosenthal cell counterpurchased from INCYTO. For Drop-Seq, an aliquot of beads was removedfrom the stock tube, washed in 500 μL of Drop-Seq Lysis Buffer (DLB, 200mM Tris pH 7.5, 6% Ficoll PM-400, 0.2% Sarkosyl, 20 mM EDTA), thenresuspended in the appropriate volume of DLB+50 mM DTT for a beadconcentration of 100 beads/μL.

Droplet generation. The two aqueous suspensions—the single-cellsuspension and the bead suspension—were loaded into 3 mL plasticsyringes containing a 6.4 mm magnetic stir disc. Droplet generation oilwas loaded into a 10 mL plastic syringe. The three syringes wereconnected to a 125 μm coflow device (FIG. 15A) by 0.38 mm inner-diameterpolyethylene tubing, and injected using syringe pumps at flow rates of4.1 mL/hr for each aqueous suspension, and 14 mL/hr for the oil,resulting in ˜125 μm emulsion drops with a volume of ˜1 nanoliter each.For movie generation, the flow was visualized under an opticalmicroscope at 10× magnification and imaged at ˜1000-2000 frames persecond using a FASTCAM SA5 color camera. Droplets were collected in 50mL falcon tubes; the collection tube was changed out for every 1 mL ofcombined aqueous flow volume to reduce the amount of soluble RNA insolution upon droplet breakage.

During droplet generation, the beads were kept in suspension bycontinuous, gentle magnetic stirring. The uniformity in droplet size andthe occupancy of beads were evaluated by observing aliquots of dropletsunder an optical microscope with bright-field illumination; in eachexperiment, greater than 95% of the bead-occupied droplets containedonly a single bead.

Droplet breakage. The oil from the bottom of each aliquot of dropletswas removed with a P1000 pipette, after which 30 mL 6×SSC at roomtemperature was added. To break droplets, Applicants added 600 μL ofPerfluoro-1-octanol, and shook the tube vigorously by hand for about 20seconds. The tube was then centrifuged for 1 minute at 1000×g. To reducethe likelihood of annealed mRNAs dissociating from the beads, the samplewas kept on ice for the remainder of the breakage protocol. Thesupernatant was removed to roughly 5 mL above the oil-aqueous interface,and the beads washed with an additional 30 mL of room temperature 6×SSC,the aqueous layer transferred to a new tube, and centrifuged again. Thesupernatant was removed, and the bead pellet transferred to non-stick1.5 mL microcentrifuge tubes. The pellet was then washed twice with 1 mLof room temperature 6×SSC, and once with 300 of 5×Maxima H- RT buffer(EP0751).

Reverse transcription and Exonuclease I treatment. To a pellet of 90,000beads, 200 μL of RT mix was added, where the RT mix contained 1× MaximaRT buffer, 4% Ficoll PM-400, 1 mM dNTPs, 1 U/μL Rnase Inhibitor, 2.5 μMTemplate Switch Oligo (Table 9), and 10 U/μL Maxima H- RT. Ficoll wasincluded to reduce settling, and because of its ability to improve RTefficiency (Lareu et al., 2007). The beads were incubated at roomtemperature for 30 minutes, followed by 42 ° C. for 90 minutes. Thebeads were then washed once with 1 mL 1× TE+0.5% Sodium Dodecyl Sulfate,twice with 1 mL TE/TW, and once with 10 mM Tris pH 7.5. The bead pelletwas then resuspended in 200 μL of exonuclease I mix containing 1×Exonuclease I Buffer and 1 U/μL Exonuclease I, and incubated at 37° C.for 45 minutes.

The beads were then washed once with 1 mL TE/SDS, twice with 1 mL TE/TW,once with 1 mL ddH₂O, and resuspended in ddH₂O. Bead concentration wasdetermined using a Fuchs-Rosenthal cell counter. Aliquots of 1000 beadswere amplified by PCR in a volume of 50 μL using 1× Hifi HotStartReadymix and 0.8 μM Template_Switch_PCR primer (Table 9).

The aliquots were thermocycled as follows: 95° C. 3 min; then fourcycles of: 98° C. for 20 sec, 65° C. for 45 sec, 72° C. for 3 min; thenX cycles of: 98° C. for 20 sec, 67° C. for 20 sec, 72° C. for 3 min;then a final extension step of 5 min. For the human-mouse experimentusing cultured cells, X was 8 cycles; for the dissociated retinaexperiment, X was 9 cycles. Pairs of aliquots were pooled together afterPCR and purified with 0.6× Agencourt AMPure XP beads according to themanufacturer's instructions, and eluted in 10 μL of H₂O. Aliquots werepooled according to the number of STAMPs to be sequenced, and theconcentration of the pool quantified on a BioAnalyzer High SensitivityChip.

Preparation of Drop-Seq cDNA library for sequencing. To prepare 3′-endcDNA fragments for sequencing, four aliquots of 600 pg of cDNA of eachsample was used as input in standard Nextera XT tagmentation reactions,performed according to the manufacturer's instructions except that 200nM of the custom primers P5_TSO_Hybrid and Nextera_N701 (Table 9) wereused in place of the kit's provided oligonucleotides. The samples werethen amplified as follows: 95° C. for 30 sec; 11 cycles of 95° C. for 10sec, 55° C. for 30 sec, 72° C. for 30 sec; then a final extension stepof 72° C. for 5 min.

Pairs of the 4 aliquots were pooled together, and then purified using0.6× Agencourt AMPure XP Beads according to the manufacturer'sinstructions, and eluted in 10 μL of water. The two 10 μL aliquots werecombined together and the concentration determined using a BioAnayzerHigh Sensitivity Chip. The average size of sequenced libraries wasbetween 450 and 650 bp.

The libraries were sequenced on the Illumina NextSeq, using 4.67 pM in avolume of 3 mL HT1, and 3 mL of 0.3 μM Read1CustSeqA or Read1CustSeqB(Table 9 and see note at the end of Extended Experimental Procedures)for priming of read 1. Read 1 was 20 bp (bases 1-12 cell barcode, bases13-20 UMI); read 2 (paired end) was 50 bp for the human-mouseexperiment, and 60 bp for the retina experiment.

Species contamination experiment. To determine the origin of off-speciescontamination of STAMP libraries (FIG. 15E), Applicants: (1) performedDrop-Seq exactly as above (control experiment) with a HEK/3T3 cellsuspension mixture of 100 cells/μL in concentration; (2) performedmicrofluidic co-flow step with HEK and 3T3 cells separately, each at aconcentration of 100 cells/μL, and then mixed droplets prior tobreakage; and (3) performed STAMP generation through exonucleasedigestion, with the HEK and 3T3 cells separately, then mixed equalnumbers of STAMPs prior to PCR amplification. A single 1000microparticle aliquot was amplified for each of the three conditions,then purified and quantified on a BioAnalyzer High Sensitivity DNA chip.600 pg of each library was used in a single Nextera Tagmentationreaction as described above, except that each of the three libraries wasindividually barcoded with the primers Nextera_N701 (condition 1),Nextera_N702 (condition 2), or Nextera_N703 (condition 3), and a totalof 12 PCR cycles were used in the Nextera PCR instead of 11. Theresulting library was quantified on a High Sensitivity DNA chip, and runat a concentration of 25 pM on the MiSeq using 0.5 μM ReadlCustSeqA as acustom primer for read 1.

Soluble RNA experiments. To quantify the number of primer annealingsites, 20,000 beads were incubated with 10 μM of polyadenylatedsynthetic RNA (synRNA, Table 9) in 2× SSC for 5 min at room temperature,and washed three times with 200 μL of TE-TW, then resuspended in 10 μLof TE-TW. The beads were then incubated at 65° C. for 5 minutes, and 1μL of supernatant was removed for spectrophotometric analysis on theNanodrop 2000. The concentration was compared with beads that had beentreated the same way, except no synRNA was added.

To determine whether the bead-bound primers were capable of reversetranscription, and to measure the homogeneity of the cell barcodesequence on the bead surface, beads were washed with TE-TW, and added ata concentration of 100/μL to the reverse transcriptase mix describedabove. This mix was then co-flowed into the standard Drop-Seq 120-micronco-flow device with 200 nM SynRNA in 1× PBS+0.02% BSA. Droplets werecollected and incubated at 42° C. for 30 minutes. 150 μL of 50 mM EDTAwas added to the emulsion, followed by 12 μL of perfluooctanoic acid tobreak the emulsion. The beads were washed twice in 1 mL TE-TW, followedby one wash in H₂O, then resuspended in TE. Eleven beads were handpickedunder a microscope into a 50 μL PCR mix containing 1× Kapa HiFi HotstartPCR mastermix, 400 nM P7-TSO_Hybrid, and 400 nM TruSeq_F (Table 9). ThePCR reaction was cycled as follows: 98° C. for 3 min; 12 cycles of: 98°C. for 20 s, 70° C. for 15 s, 72° C. for 1 min; then a final 72° C.incubation for 5 min. The resulting amplicon was purified on a Zymo DNAClean and Concentrator 5 column, and run on a BioAnalyzer HighSensitivity Chip to estimate concentration. The amplicon was thendiluted to 2 nM and sequenced on an Illumina MiSeq. Read 1, primed usingthe standard Illumina TruSeq primer, was a 20 bp molecular barcode onthe SynRNA, while Read 2, primed with CustSynRNASeq, contained the 12 bpcell barcode and 8 bp UMI.

To estimate the efficiency of Drop-Seq, Applicants used a set ofexternal RNAs. Applicants diluted the ERCC spike-ins to 0.32% of thestock in 1× PBS+1 U/μL RNase Inhibitor+200 μg/ mL BSA (NEB), and usedthis in place of the cell flow in the Drop-Seq protocol, so that eachbead was incubated with ˜100,000 ERCC mRNA molecules per nanoliterdroplet. Sequence reads were aligned to a dual ERCC-human (hg19)reference, using the human sequence as “bait,” which dramaticallyreduced the number of low-quality alignments to ERCC transcriptsreported by STAR compared with alignment to an ERCC-only reference.

Standard mRNA-seq. To compare Drop-Seq average expression data tostandard mRNAseq data, Applicants used 1.815 ug of purified RNA from 3T3cells, from which Applicants also prepared and sequenced 550 STAMPs. TheRNA was used in the TruSeq Stranded mRNA Sample Preparation kitaccording to the manufacturer's instructions. For NextSeq 500sequencing, 0.72 pM of Drop-Seq library was combined with 0.48 pM of themRNAseq library.

In-solution template switch amplification. To compare Drop-Seq averageexpression data to mRNAseq libraries prepared by a standard, in-solutiontemplate switch amplification approach, 5 ng of purified RNA from 3T3cells, from which Applicants also prepared and sequenced 550 STAMPs, wasdiluted in 2.75 μl of H₂O. To the RNA, 1 μl of 10 μM UMI_SMARTdT primerwas added (Table 9) and heated to 72° C., followed by incubation at 4°C. for 1 min, after which Applicants added 2 μl 20% Ficoll PM-400, 2 μl5× RT Buffer (Maxima H- kit), 1 μl 10 mM dNTPs, 0.5 μl 50μMTemplate_Switch_Oligo (Table 9), and 0.5 μl Maxima H-RT. The RT wasincubated at 42° C. for 90 minutes, followed by heat inactivation for 5min at 85° C. An RNase cocktail (0.5 μl RNase I, Epicentre N6901K, and0.5 μl RNase H) was added to remove the terminal riboGs from thetemplate switch oligo, and the sample incubated for 30 min at 37° C.Then, 0.4 μl of M Template_Switch_PCR primer was added, along with 25 μl2× Kapa Hifi supermix, and 13.6 μl H₂O. The sample was cycled asfollows: 95° C. 3 min; 14 cycles of: 98° C. 20 s, 67° C. 20 s, and 72°C. 3 min; then 72° C. 5 min. The samples were purified with 0.6 AMPureXP beads according to the manufacturer's instructions, and eluted in 10μl. 600 pg of amplified cDNA was used as input into a Nextera XTreaction. 0.6 pM of library was sequenced on a NextSeq 500, multiplexedwith three other samples; ReadlCustSeqB was used to prime read 1.

Droplet digital PCR (ddPCR) experiments. To quantify the efficiency ofDrop-Seq, 50,000 HEK cells, prepared in an identical fashion as inDrop-Seq, were pelleted and RNA purified using the Qiagen RNeasy PlusKit according to the manufacturer's protocol. The eluted RNA was dilutedto a final concentration of 1 cell-equivalent per microliter in anRT-ddPCR reaction containing RT-ddPCR supermix, and a gene primer-probeset. Droplets were produced using BioRad ddPCR droplet generationsystem, and thermocycled with the manufacturer's recommended protocol,and droplet fluorescence analyzed on the BioRad QX100 droplet reader.Concentrations of RNA and confidence intervals were computed by BioRadQuantaSoft software. Three replicates of 50,000 HEK cells were purifiedin parallel, and the concentration of each gene in each replicate wasmeasured two independent times. The probes used were: ACTB(hs01060665_g1), B2M (hs00984230_m1), CCNB1 (mm03053893), EEF2(hs00157330_m1), ENO1 (hs00361415_m1), GAPDH (hs02758991_g₁), PSMB4(hs01123843_g1), TOP2A (hs01032137_m1), YBX3 (hs01124964_m1), and YWHAH(hs00607046_m1).

To estimate the RNA hybridization efficiency of Drop-Seq, human braintotal RNA was diluted to 40 ng/μl in a volume of 20 μl and combined with20 μl of barcoded primer beads resuspended in Drop-Seq lysis buffer(DLB, composition shown below) at a concentration of 2,000 beads/μl .The solution was incubated at 15 minutes with rotation, then spun downand the supernatant transferred to a fresh tube. The beads were washed 3times with 100 μl of 6× SSC, resuspended in 50 μH2O, and heated to 72°C. for 5 min to elute RNA off the beads. The elution step was repeatedonce and the elutions pooled. All steps of the hybridization (RNA input,hybridization supernatant, three washes, and combined elution) wereseparately purified using the Qiagen RNeasy Plus Mini Kit according tothe manufacturers' instructions. Various dilutions of the elutions wereused in RT-ddPCR reactions with primers and probes for either ACTB orGAPDH.

Fluidigm C1 experiments. C1 experiments were performed as previouslydescribed (Shalek et al., 2014). Briefly, suspensions of 3T3 and HEKcells were stained with calcein violet and calcein orange (LifeTechnologies) according to the manufacturer's recommendations, diluteddown to a concentration of 250,000 cells per mL, and mixed 1:1. Thiscell mixture was then loaded into two medium C1 cell capture chips fromFluidigm and, after loading, caught cells were visualized and identifiedusing DAPI and TRITC fluorescence. Bright field images were used toidentify ports with >1 cell (a total of 12 were identified from the twoC1 chips used, out of 192 total). After C1-mediated whole transcriptomeamplification, libraries were made using Nextera XT (Illumina), andloaded on a NextSeq 500 at 2.2 pM. Single-read sequencing (60 bp) wasperformed to mimic the read structure in DropSeq, and the reads alignedas per below,

Read alignment and generation of digital expression data. Raw sequencedata was first filtered to remove all read pairs with a barcode basequality of less than 10. The second read (50 or 60 bp) was then trimmedat the 5′ end to remove any TSO adapter sequence, and at the 3′ end toremove polyA tails of length 6 or greater, then aligned to either themouse (mm10) genome (retina experiments) or a combined mouse (mm10)-human (hg19) mega-reference, using STAR v2.4.0 a with default setting.

Uniquely mapped reads were grouped by cell barcode. To digitally countgene transcripts, a list of UMIs in each gene, within each cell, wasassembled, and UMIs within ED=1 were merged together. The total numberof unique UMI sequences was counted, and this number was reported as thenumber of transcripts of that gene for a given cell.

To distinguish cell barcodes arising from STAMPs, rather than those thatcorresponded to beads never exposed to cell lysate, Applicants orderedthe digital expression matrix by the total number of transcripts percell barcode, and plotted the cumulative fraction of all transcripts inthe matrix for each successively smaller cell barcode. Empirically,Applicants' data always displays a “knee,” at a cell barcode numberclose to the estimate number of STAMPs amplified (FIG. 14B). All cellbarcodes larger than this cutoff were used in downstream analysis, whilethe remaining cell barcodes were discarded.

Cell cycle analysis of HEK and 3T3 cells. Gene sets reflecting fivephases of the HeLa cell cycle (G1/S, S, G2/M, M and M/G1) were takenfrom Whitfield et al. (Whitfield et al., 2002) (Table 3), and refined byexamining the correlation between the expression pattern of each geneand the average expression pattern of all genes in the respectivegene-set, and excluding genes with a low correlation (R<0.3). This stepremoved genes that were identified as phase-specific in Hela cells butdid not correlate with that phase in Applicants' single cell data. Theremaining genes in each refined gene-set were highly correlated (notshown). Applicants then averaged the normalized expression levels(log₂(TPM+1)) of the genes in each gene-set to define the phase-specificscores of each cell. These scores were then subjected to twonormalization steps. First, for each phase, the scores were centered anddivided by their standard deviation. Second, the normalized scores ofeach cell were centered and normalized.

To order cells according to their progression along the cell cycle,Applicants first compared the pattern of phase-specific scores, of eachcell, to eight potential patterns along the cell cycle: only G1/S is on,both G1/S and S, only S, only G2/M, G2/M and M, only M, only M/G1, M/G1and G1. Applicants also added a ninth pattern for equal scores of allphases (either all active or all inactive). Each pattern was definedsimply as a vector of ones for active programs and zeros for inactiveprograms. Applicants then classified the cells to the defined patternsbased on the maximal correlation of the phase-specific scores to thesepotential patterns. Importantly, none of the cells were classified tothe ninth pattern of equal activity, while multiple cells wereclassified to each of the other patterns. To further order the cellswithin each class Applicants sorted the cells based on their relativecorrelation with the preceding and succeeding patterns, therebysmoothing the transitions between classes (FIG. 10A).

To identify cell cycle-regulated genes Applicants used the cell cycleordering defined above and a sliding window approach with a window sizeof 100 cells. Applicants identified the windows with maximal averageexpression and minimal average expression for each gene and used atwo-sample t-test to assign an initial p-value for the differencebetween maximal and minimal windows. A similar analysis was performedafter shuffling the order of cells in order to generate control p-valuesthat can be used to evaluate false-discovery rate (FDR). Specifically,Applicants examined for each potential p-value threshold, how many genespass that threshold in the cell-cycle ordered and in therandomly-ordered analyses to assign FDR. Genes were defined as beingpreviously known to be cell-cycle regulated if they were included in acell cycle GO/KEGG/REACTOME gene set, or reported in a recentgenome-wide study of gene expression in synchronized replicating cells(Bar-Joseph et al., 2008).

Unsupervised dimensionality reduction and clustering analysis of retinadata. P14 mouse retina suspensions were processed through Drop-Seq inseven different replicates on four separate days, and each sequencedseparately. Raw digital expression matrices were generated for the sevensequencing runs. The inflection points (number of cells) for each samplereplicate were as follows: 6,600, 9,000, 6,120, 7,650, 7,650, 8280, and4000. The full 49,300 cells were merged together in a single matrix, andfirst normalized by the number of UMIs by dividing by the total numberof UMIs per cell, then multiplied by 10,000. All calculations and datawere then performed in log space (i.e. ln(transcripts-per-10,000+1)).

Initial downsampling and identification of highly variable genes. Rodphotoreceptors constitute 60-70% of the retinal cell population.Furthermore, they are significantly smaller than other retinal celltypes (Carter-Dawson and LaVail, 1979), and as a result yieldedsignificantly fewer genes (and higher levels of noise) in Applicants'single cell data. In Applicants' preliminary computational experiments,performing unsupervised dimensionality reduction on the full datasetresulted in representations that were dominated by noisy variationwithin the numerous rod subset; this compromised Applicants' ability toresolve the heterogeneity within other cell-types that werecomparatively smaller in frequency (e.g. amacrines, microglia). Thus, toincrease the power of unsupervised dimensionality reduction techniquesfor discovering these types Applicants first downsampled the 49,300-celldataset to extract single-cell libraries where 900 or more genes weredetected, resulting in a 13,155-cell “training set”. Applicantsreasoned. that this “training set” would be enriched for rare cell typesthat are larger in size at the expense of “noisy” rod cells. Theremaining 36,145 cells (henceforth “projection set”) were then directlyembedded onto to the low dimensional representation learned from thetraining set (see below). This enabled us to leverage the fullstatistical power of Applicants' data to define and annotate cell types.

Applicants first identified the set of genes that was most variableacross the training set, after controlling for the relationship betweenmean expression and variability. Applicants calculated the mean and adispersion measure (variance/mean) for each gene across all 13,155single cells, and placed genes into 20 bins based on their averageexpression. Within each bin, Applicants then z-normalized the dispersionmeasure of all genes within the bin, in order to identify outlier geneswhose expression values were highly variable even when compared to geneswith similar average expression. Applicants used a z-score cutoff of 1.7to identify 384 significantly variable genes, which as expected,consisted of markers for distinct retinal cell types.

Principal Components Analysis. Applicants ran Principal ComponentsAnalysis (PCA) on Applicants' training set as previously described(Shalek et al., 2013), using the prcomp function in R, after scaling andcentering the data along each gene. Applicants used only the previouslyidentified “highly variable” genes as input to the PCA in order toensure robust identification of the primary structures in the data.

While the number of principal components returned is equal to the numberof profiled cells, only a small fraction of these components explain astatistically significant proportion of the variance, as compared to anull model. Applicants used two approaches to identify statisticallysignificant PCs for further analysis: (1) Applicants performed 10000independent randomizations of the data such that within eachrealization, the values along every row (gene) of the scaled expressionmatrix are randomly permuted. This operation randomizes the pairwisecorrelations between genes while leaving the expression distribution ofevery gene unchanged. PCA was performed on each of these 10000“randomized” datasets. Significant PCs in the un-permuted data wereidentified as those with larger eigenvalues compared to the highesteigenvalues across the 10000 randomized datasets (p<0.01, Bonferronicorrected). (2) Applicants modified a randomization approach (‘jackstraw’) proposed by Chung and Storey (Chung and Storey, 2014) and whichApplicants have previously applied to single-cell RNA-seq data (Shaleket al., 2014), Briefly, Applicants performed 1,000 PCAs on the inputdata, but in each analysis, Applicants randomly ‘scrambled’ 1% of thegenes to empirically estimate a null distribution of scores for everygene. Applicants used the joint-null criterion (Leek and Storey, 2011)to identify PCs that had gene scores significantly different from therespective null distributions (p<0.01, Bonferroni corrected), Both (1)and (2) yielded 32 ‘significant’ PCs. Visual inspection confirmed thatnone of these PCs was primarily driven by mitochondrial, housekeeping,or hemoglobin genes. As expected, markers for distinct retinal celltypes were highly represented among the genes with the largest scores(+ve and −ve) along these PCs (Table 5).

t-SNE representation and post-hoc projection of remaining cells. Becausecanonical markers for different retinal cell types were stronglyrepresented along the significant PCs (FIG. 17), Applicants reasonedthat the loadings for individual cells in the training set along theprincipal eigenvectors (also “PC subspace representation”) could be usedto separate out distinct cell types in the data. Applicants note thatthese loadings leverage information from the 384 genes in the PCA, andtherefore are more robust to technical noise than single-cellmeasurements of individual genes. Applicants used these PC loadings asinput for t-Distributed Stochastic Neighbor Embedding (tSNE) (van derMaaten and Hinton, 2008), as implemented in the tsne package in R withthe “perplexity” parameter set to 30. The t-SNE procedure returns atwo-dimensional embedding of single cells. Cells with similar expressionsignatures of genes within Applicants' variable set, and thereforesimilar PC loadings, will likely localize near each other in theembedding, and hence distinct cell types should form two-dimensionalpoint clouds across the tSNE map.

Prior to identifying and annotating the clusters, Applicants projectedthe remaining 36,145 cells (the projection set) onto the tSNE map of thetraining set by the following procedure:

-   -   (1) Applicants projected these cells onto the subspace defined        by the significant PCs identified from the training set.        Briefly, Applicants centered and scaled the 384×36,145        expression matrix corresponding to the projection set,        considering only the highly variable genes; the scaling        parameters of training set were used to center and scale each        row. Applicants then multiplied the transpose of this scaled        expression matrix with the 384×32 gene scores matrix learned        from the training set PCA. This yields a PC “loadings” for the        cells in the projection set along the 32 significant PCs learned        on the training set.    -   (2) Based on its PC loadings, each cell in the projection set        was independently embedded on to the tSNE map of the training        set introduced earlier using a mathematical framework consistent        with the original tSNE algorithm (Shekhar et al., 2014).        Applicants note that while this approach does not discover novel        clusters outside of the ones identified from the training set,        it sharpens the distinctions between different clusters by        leveraging the statistical power of the full dataset. Moreover,        the cells are projected based on their PC signatures, not the        raw gene expression values, which makes Applicants' approach        more robust against technical noise in individual gene        measurements.

See section “Embedding the projection set onto the tSNE map” below forfull details.

One potential concern with this “post-hoc projection approach” was thepossibility that a cell type that is completely absent from the trainingset might be spuriously projected into one of the defined clusters.Applicants tested the projection algorithm on a control dataset toexplore this possibility, and placed stringent conditions to ensure thatonly cell types adequately represented within the training set areprojected to avoid spurious assignments (see ‘“Out of sample” projectiontest’). Using this approach, 97% of the cells in the projection set weresuccessfully embedded, resulting in a tSNE map consisting of 48296 outof 49300 sequenced cells (Table 10).

As an additional validation of Applicants' approach, it was noted thatthe relative frequencies of different cell types identified afterclustering the full data (see below) closely matches estimates in theliterature (Table 1). With the exception of the rods, all the othercell-types were enriched at a median value of 2.3× in the training setcompared to their frequency of the full data. This strongly suggeststhat Applicants' downsampling approach indeed increases therepresentation of other cell types at the expense of the rod cells,enabling us to discover PCs that define these cells.

Density clustering to identify cell-types. To automatically identifyputative cell types on the tSNE map, Applicants used a densityclustering approach implemented in the DBSCAN R package (Ester et al.,1996), setting the reachability distance parameter (eps) to 1.9, andremoving clusters less than 50 cells. The majority of the removed cellsincluded singleton cells that were located between the interfaces ofbigger clusters. As a result of these steps, Applicants were able toassign 44808 cells (91% of the data) into 49 clusters.

Applicants next examined the 49 total clusters, to ensure that theidentified clusters truly represented distinct cellular classifications,as opposed to over-partitioning. Applicants performed a post-hoc testwhere Applicants searched for differentially expressed genes (McDavid etal., 2013) between every pair of clusters (requiring at least 10 genes,each with an average expression difference greater than 1 natural logvalue between clusters with a Bonferroni corrected p<0.01). Applicantsiteratively merged cluster pairs that did not satisfy this criterion,starting with the two most related pairs (lowest number ofdifferentially expressed genes). This process resulted in 10 mergedclusters, leaving 39 remaining.

Applicants then computed average gene expression for each of the 39remaining clusters, and calculated Euclidean distances between allpairs, using this data as input for complete-linkage hierarchicalclustering and dendrogram assembly. Applicants then compared each of the39 clusters to the remaining cells using a likelihood-ratio test(McDavid et al., 2013) to identify marker genes that were differentiallyexpressed in the cluster.

Embedding the projection set onto the tSNE map. Applicants used thecomputational approach in Shekhar et al (Shekhar et al., 2014) andBerman et al. (Berman et al., 2014) to project new cells onto anexisting tSNE map. First, the expression vector of the cell is reducedto include only the set of highly variable genes, and subsequentlycentered and scaled along each gene using the mean and standarddeviation of the gene expression in the training set. This scaledexpression vector z (dimensions 1×384) is multiplied with the scoresmatrix of the genes S (dimensions 384×32), to obtain its “loadings”along the significant PCs u (dimensions 1×32). Thus, u′=z′.S

u (dimensions 1×32) denotes the representation of the new cell in the PCsubspace identified from the training set. Applicants note a point ofconsistency here in that performing the above dot product on a scaledexpression vector of a cell z taken from the training set recovers itscorrect subspace representation u, as it ought to be the case.

Given the PC loadings of the cells in the training set {u′} (1=1,2, . .. N_(train)) and their tSNE coordinates {y^(i)} (i=1, 2, . . .N_(train)), the task now is to find the tSNE coordinates y′ of the newcell based on its loadings vector u′. As in the original tSNE framework(van der Maaten and Hinton, 2008), Applicants “locate” the new cell inthe subspace relative to the cells in the training set by computing aset of transition probabilities,

${p\left( u^{\prime} \middle| u^{i} \right)} = \frac{\exp \left( {{{- {d\left( {u^{\prime},u^{i}} \right)}^{2}}/2}\sigma_{u^{\prime}}^{2}} \right)}{\sum_{\{ u^{i}\}}{\exp \left( {{{- {d\left( {u^{\prime},u^{i}} \right)}^{2}}/2}\sigma_{u^{\prime}}^{2}} \right)}}$

Here, d( . , . ) represents Euclidean distances, and the the bandwidthσ_(u′) is chosen by a simple binary search in order to constrain theShannon entropy associated with p(u′|u^(i)) to log₂(30), where 30corresponds to the value of the perplexity parameter used in the tSNEembedding of the training set. Note that σ_(u′) is chosen independentlyfor each cell.

A corresponding set of transition probabilities in the low dimensionalembedding are defined based on the Student's t-distribution as,

${q\left( y^{\prime} \middle| y^{i} \right)} = \frac{\left( {1 + {d\left( {y^{\prime},y^{i}} \right)}^{2}} \right)^{- 1}}{\sum_{\{ y^{i}\}}\left( {1 + {d\left( {y^{\prime},y^{i}} \right)}^{2}} \right)^{- 1}}$

where y′ are the coordinates of the new cell that are unknown.Applicants calculate these by minimizing the Kullback-Leibler divergencebetween p(u′|u^(i)) and q(y′|y^(i)),

$y^{\prime} = {\arg \; \min {\sum\limits_{i}{{p\left( u^{\prime} \middle| u^{i} \right)}\log \frac{p\left( u^{\prime} \middle| u^{i} \right)}{q\left( y^{\prime} \middle| y^{i} \right)}}}}$

This is a non-convex objective function with respect to its arguments,and is minimized using the Nelder-Mead simplex algorithm, as implementedin the Matlab function fminsearch. This procedure can be parallelizedacross all cells in the projection set.

A few notes on the implementation,

-   -   1. Since this is a post-hoc projection, and p(u′|u^(i)) is only        a relative measure of pairwise similarity in that it is always        constrained to sum to 1, Applicants wanted to avoid the        possibility of new cells being embedded on the tSNE map by        virtue of their high relative similarity to one or two training        cells (“short circuiting”). In other words, Applicants chose to        project only those cells that were drawn from regions of the PC        subspace that were well represented in the training set by at        least a few cells. Thus, Applicants retained a cell u′ for        projection only if p(u′|u^(i))>p_(thres) was true for at least        N_(min) cells in the training set (p_(thres)=5×10⁻³,        N_(min)=10). Applicants calibrated the values for p_(thres) and        N_(min) by testing the projection algorithm on cases where the        projection set was known to be completely different from the        training set to ensure that such cells were largely rejected by        this constraint. (see Section ‘“Out of sample” projection test’)    -   2. For cells that pass the constraint in pt. 1., the initial        value of the tSNE coordinate y′₀ is set to,

$y_{0}^{\prime} = {\sum\limits_{i}{{p\left( u^{\prime} \middle| u^{i} \right)}y^{i}}}$

i.e. a weighted average of the tSNE coordinates of the training set withthe weights set to the pairwise similarity in the PC subspacerepresentation.

-   -   3. A cell satisfying the condition in 1. is said to be        “successfully projected” to a location y′* when a minimum of the        KL divergence could be found within the maximum number of        iterations. However since the program is non-convex and is        guaranteed to only find local minima, Applicants wanted to        explore if a better minima could be found. Briefly, Applicants        uniformly sampled points from a 25×25 grid centered on y′* to        check for points where the value of the KL-divergence was within        5% of its value at y′* or lower. Whenever this condition was        satisfied (<2%) of the time, Applicants re-ran the optimization        by setting the new point as the initial value.

“Out of sample” projection test. In order to test the post-hocprojection method, Applicants conducted the following computationalexperiment wherein each of the 39 distinct clusters on the tSNE map wassynthetically “removed” from the tSNE map, and then reprojectedcell-by-cell on the tSNE map of the remaining clusters using theprocedure outlined above. Only cells from the training set were used inthese calculations.

Assuming Applicants' cluster distinctions are correct, in each of these39 experiments, the cluster that is being reprojected represents an “outof sample” cell type. Thus successful assignments of these cells intoone of the remaining 38 clusters would be spurious. For each of the 39clusters that was removed and reprojected, Applicants classified thecells into three groups based on the result of the projection method

-   -   (1) Cells that did not satisfy the condition 1. in the previous        section (i.e. did not have a high relative similarity to at        least N_(min) training cells), and therefore “failed” to        project.    -   (2) Cells that were successfully assigned a tSNE coordinate y′,        but that could not be assigned into any of the existing clusters        according to the condition below.    -   (3) Cells that were successfully assigned a tSNE coordinate y′,        and which were “wrongly assigned” to one of the existing        clusters. A cell was assigned to a cluster whose centroid was        closest to y′ if and only if the distance between y′ and the        centroid was smaller than the cluster radius (the distance of        the farthest point from the centroid).

Encouragingly for all of the 39 “out of sample” projection experiments,only a small fraction of cells were spuriously assigned to one of theclusters, i.e. satisfied (3) above with the parameters p_(thres)=5×10⁻³and N_(min)=10 (Table 10). This provided confidence that

Applicants' post-hoc embedding of the projection set would notspuriously assign distinct cell types into one of the existing clusters.

Downsampling analyses of retina data. To generate the 500-cell and2000-cell downsampled tSNE plots shown in FIG. 11F, cells were randomlysampled from the high-purity replicate (replicate 7), and used as inputfor PCA and tSNE. The 500-cell tSNE was clustered using a reachabilitydistance parameter (eps) of 5.5, while the 2000-cell tSNE was clusteredusing an eps value of 3.0. Unclustered cells were removed. To generatethe 9,431-cell downsampled tSNE plot, 10,000 cells were randomly sampledfrom the full dataset, and the cells expressing transcripts from morethan 900 genes were used in principal components analysis and tSNE; theremaining (smaller) cells were projected onto the tSNE embedding, andclustered using an eps value of 2.0, resulting in a plot with 9,431cells.

Immunohistochemistry. Wild-type C57 mice or Mito-P mice, which expressCFP in nGnG amacrine and Type 1 bipolar cells (Kay et al.. 2011), wereeuthanized by intraperitoneal injection of pentobarbital. Eyes werefixed in 4% PFA in PBS on ice for one hour, followed by dissection andpost-fixation of retinas for an additional 30 mins, then rinsed withPBS. Retinas were frozen and sectioned at 20 μm in a cryostat. Sectionswere incubated with primary antibodies (chick anti-GFP [Abcatn] orrabbit anti-PPPiR17 [Atlas]) overnight at 4° C., and with secondaryantibodies (INvitrogen and Jackson ImmunoResearch) for 2 hrs at roomtemperature. Sections were then mounted using Fluoromount G (SouthernBiotech) and viewed with an Olympus FVB confocal microscope.

Note on bead surface primers and custom sequencing primers. During thecourse of experiments for this paper, Applicants used two batches ofbeads that had two slightly, different sequences (Barcoded Bead SeqA andBarcoded Bead SeqB, Table 9). Barcoded Bead SeqA was used in thehuman-mouse experiments, and in replicates 1-3 of the retina experiment.Replicates 4-7 were performed with Barcoded Bead SeqB. To prime read 1for Drop-Seq libraries produced using Barcoded Bead SeqA beads,ReadlCustSeqA was used; to prime read 2 for Drop-Seq libraries producedusing Barcoded Bead SeqB beads, ReadlCustSeqB was used. ChemGenes plansto manufacture large-scale numbers of beads harboring the Barcoded BeadSeqB sequence. These beads should be used with ReadlCustSeqB.

Additional notes regarding Drop-Seq implementation

Cell and bead concentrations. Applicants' experiments have shown thatthe cell concentration used in Drop-Seq has a strong, linearrelationship to the purity and doublet rates of the resulting libraries(FIGS. 9A, 9B, and 14D). Cell concentration also linearly affectsthroughput: ˜10,000 single-cell libraries can be processed per hour whencells are used at a final concentration of 100 cells/ul, and ˜1,200 canbe processed when cells are used at a final concentration of 12.5cells/ul. The trade-off between throughput and purity is likely toaffect users differently, depending on the specific scientific questionsbeing asked. Currently, for the standard experiments, Applicants use afinal concentration of 50 cells/ul, tolerating a small percentage ofdoubles and cell contaminants, to be able to easily and reliably process10,000 cells over the course of a couple of hours. As recommended above,Applicants currently favor loading beads at a concentration of 120/ul(final concentration in droplets=60/ul), which empirically yields a <5%bead doublet rate.

Drop-Seq start-up costs. The main pieces of equipment required toimplement Drop-Seq are three syringe pumps (KD Legato 100 pumps, listprice ˜2,000 each) a standard inverted microscope (Motic AE31, listprice $1,900), and a magnetic stirrer (V&P scientific, #710D2, listprice ˜$1,200). A fast camera (used to monitor droplet generation inreal time) is not necessary for the great majority of users (dropletquality can easily be monitored by simply placing 3 ul of droplets in aFuchs-Rosenthal hemocytometer with 17 ul of droplet generation oil todilute the droplets into a single plane of focus).

Example 4 Tables for Examples 2 and 3

TABLE 1 Ascertainment of cell types and frequencies in the mouse retinaby Drop-Seq. The sizes of the 39 annotated cell clusters produced fromDrop-Seq were used to estimate their fractions of the total cellpopulation. These data were compared with those obtained by microscopytechniques (Jeon et al., 1998). Percentage of retina Percentage of (Jeonet al., cell population Cell class 1998) (%) in Drop-Seq (%) Rodphotoreceptors 79.9 65.6 Cone photoreceptors 2.1 4.2 Muller glia 2.8 3.6Retinal ganglion cells 0.5 1.0 Horizontal cells 0.5 0.6 Amacrine cells7.0 9.9 Bipolar cells 7.3 14 Microglia — 0.2 Retinal endothelial — 0.6cells Astrocytes 0.1

TABLE 1 Edit distance relationships among UMIs. For the data in FIG. 3G,the sequences of the UMIs for each ERCC gene detected in each cellbarcode were collapsed at an edit distance of 1, including onlysubstitutions (left column) or with both substitutions andinsertions/deletions (right column). A control UMI set was prepared foreach gene, using an equal number of UMIs sampled randomly across allgenes/cells. The percent of the original UMIs that were collapsed foreach condition are reported in the table. UMI % Reduction in UMI countsSampling Substitution-only collapse Indel and substitution collapseWithin a 68.2% 76.1% gene Across genes 19.1% 45.7%

TABLE 2 Top 100 genes represented in each of the first 5 principalcomponents calculated from the human (HEK) single-cell expression data.PC1 PC2 PC3 PC4 PC5 OPTN CENPE MT-RNR2 CCNB1 PAPOLA H1F0 CENPF DDX21PSRC1 DTL CREBRF KIF14 GPATCH4 CDC20 TAF7 RHOU TPX2 WDR43 AURKA RTN4NEAT1 TOP2A LYAR PLK1 TOP1 PRSS23 AURKA FAM211A CKS2 CDCA7 RIT1 DLGAP5MYBBP1A KIF20A E2F3 CDKN1A DEPDC1 GNL3 HMMR HSP90AA1 MAF SGOL2 NCL PTTG1TUG1 MALAT1 PRC1 RSL1D1 CENPA HSPH1 CCNE2 CCNB1 RPF2 CDCA3 DYNLL1 DDIT3ASPM MYC BUB1 ZNF367 MAP1A ARL6IP1 DKC1 CCNB2 MORF4L2 MTRNR2L12 HMMRLARP1 TUBA1C AASDHPPT PPP1R15A PLK1 NOP58 PIF1 HNRNPH3 ATXN1 MALAT1CD3EAP DEPDC1 HSP90AB1 DGCR8 MKI67 SLC6A15 SGOL2 HIST1H2AC MT-RNR2 CDCA3PA2G4 KIF2C KTN1 TES TTK NOP14 AURKB ZRANB2 FNIP1 CDC20 SNHG3 TIMM10HIST1H2BD SAT1 SMC4 DNAJC2 TPX2 ZNF738 ZNF608 BUB1 HEATR1 TUBB4B PSMD10WDR76 CKS2 NOP16 CENPE PSMD14 NFIB TACC3 NOP56 CDCA8 SET ERO1LB CKAP2SET UBE2C SSB MXD1 GTSE1 PUS7 G2E3 EIF4G2 TSPYL4 CKAP5 WDR3 GOT1 PIGWARID4A ANLN RRP15 RNF26 HNRNPR HOXA3 G2E3 MTRNR2L12 FAM64A FUBP1 DDAH2NCAPG NOLC1 GAS2L3 SNHG3 CLU KIF18A QTRTD1 NDC80 ZC3H15 FAM46A NDC80LTV1 TMEM115 PAIP2 ARID5B HMGB2 MRTO4 XRCC4 DHX29 IFI27L2 CDCA8 SCDFAM83D HSP90B1 SCN9A PIF1 NOB1 NAMPTL ATP6V1G1 KCTD7 UBE2C SLC16A1MPV17L2 HNRNPH2 TTLL7 NUF2 POLR3G KPNA2 GOLM1 PCDH17 KIF20A KCTD12ARL6IP1 CMTM6 PLAT KPNA2 SLC1A3 DHRS7B HNRNPU NAB1 KIF11 MTRNR2L8 PRC1CAP1 CAPRIN2 KIF23 PAK1IP1 CDKN3 STIP1 LYPD1 KIF4A MT-ND5 HSPA1B JAK1TMSB4X SFPQ NOL8 TACC3 QKI N4BP2 PSRC1 MT-ND2 BUB1B PFDN4 TM7SF2 BUB1BDHX37 INCENP MIS18A TMEM107 KIF20B UTP14A DTWD2 MSH6 ZNF226 KDM5B DPH2SAPCD2 PPP1CB PHTF1 BIRC5 MTRNR2L1 CCDC86 C11orf58 MTRNR2L8 HP1BP3 NPM1KRT10 ZNF280B MTRNR2L3 CASC5 NOC3L TRMT61B DNAJA1 DLG3 BRD8 FASN DYNLL1EID1 TMSB15A PRRC2C SERBP1 DEPDC1B FAM200B UHRF1 CENPA TSR1 MGARP RDXGATA6 NUSAP1 RIOK1 EIF1 VBP1 NOVA1 DBF4 MT-RNR1 PPP1R11 ANP32E C22orf46CALM2 RRS1 CUTC SKIL RFX7 INCENP NAA15 TTK PTTG1 ZNF280B ECT2 WDR4 PEX3CSNK1A1L GKAP1 EIF4G3 TAF1D MRPL12 RAB7A CYP1B1 KIF5B UTP20 CDC25BCTNNB1 ZNF107 C6orf62 TNPO2 DNAJC17 CHMP5 LRRCC1 NIPBL CDK6 PPM1BPRPF40A ZNF200 CEP350 ST6GALNAC2 HN1 MRFAP1 DTL PRR11 NAA25 CALM2 INAOTUD7B CKAP2L FAM216A BRI3 ARCN1 ULK1 CCDC18 TCOF1 SAP30 NUP37 HIST1H2BJCEP70 C10orf2 PSMF1 ENAH MED13L RBBP6 HRK ECT2 STK32C WEE1 ARID4B RRP1BSPAG5 SNRPB2 RAB9B KIF2C NOP2 MED30 DYNC1I2 SIPA1L2 SGOL1 BCAT1 TNIP2CFL2 FADS2 CCNB2 AMD1 DUSP14 BTF3 ZDBF2 ACIN1 MIR17HG TMEM99 TIPIN KIF1ACDC27 POLR1A RAB28 ARV1 ATF3 U2SURP MDN1 BIRC5 NACA GADD45A ARHGAP11ARRP12 DOHH CHMP2B NEXN CCNA2 PWP1 MAD2L1 ILF2 PPP1R9A CDKN1B RCC1 BOLA1RPL5 BNIP3L TRA2A GRB14 C14orf119 SLTM C4orf21 RSF1 C8orf33 DCPS NAP1L3NPHP3 DR1 MTHFD1L PDIA5 PIK3R3 TRPS1 TUBB4B AKAP1 SART1 ADAR COLEC12BOD1L1 POU3F2 MRPS2 HNRNPK ZFHX3 NCAPD2 TTLL12 MIOS CAPRIN1 SNAPC5 KIF4BFAM208B CSTB METAP2 REV3L CDCA2 EIF5B RANGAP1 CSNK1A1 REST USP9X CEBPZTFCP2 NCKAP1 ANKRD12 RANGAP1 STARD7 MAP7D1 CBX1 YPEL5 SON CDV3 CETN3CDV3 UBE2H CCAR1 PNO1 GTPBP6 KRR1 SERPINB1 TNRC6B ABCE1 RACGAP1 KPNA4ZNF367 GOLGA4 JSRP1 CKAP5 HMMR SMARCA1 SRRM2 PAWR SPR TMEM167A BAZ2B LBRTIMM44 SAMD8 MMADHC SESN3 PTTG1 TWISTNB MRPL3 ISCU C1orf63 NEK2 TFRCFBXO38 NACA2 HOXA-AS4 AURKB MT-ND4 ZNRD1 FXR1 ZFP90 RBMX IPO7 CENPFHSPA14 NFAT5 HEXIM1 MTPAP C8orf76 PSMD4 ZNF711 CCDC88A HSPD1 PES1 MARCH5

TABLE 3 Genes used for each phase of the cell cycle for the analysis inFIG. 4. G1/S S G2/M M M/G1 ACD ABCC5 ANLN AHI1 AGFG1 ACYP1 ABHD10 AP3D1AKIRIN2 AGPAT3 ADAMTS1 ANKRD18A ARHGAP19 ANKRD40 AKAP13 ANKRD10 ASF1BARL4A ANLN AMD1 APEX2 ATAD2 ARMC1 ANP32B ANP32E ARGLU1 BBS2 ASXL1 ANP32EANTXR1 ATAD2 BIVM ATL2 ARHGAP19 BAG3 BARD1 BLM AURKB ARL6IP1 BTBD3 BRD7BMI1 BCLAF1 ASXL1 CBX3 C1orf63 BRCA1 BORA ATF7IP CDC42 C7orf41 BRIP1BRD8 AURKA CDK7 C14orf142 C5orf42 BUB3 BIRC2 CDKN3 CAPN7 C11orf82C2orf69 BIRC5 CEP70 CASP2 CALD1 C14orf80 BUB1 CNIH4 CASP8AP2 CALM2 CASP3CADM1 CTR9 CCNE1 CASP2 CBX5 CCDC88A CWC15 CCNE2 CCDC14 CCDC107 CCDC90BDCP1A CDC6 CCDC84 CCNA2 CCNA2 DCTN6 CDC25A CCDC150 CCNF CCNB2 DEXI CDCA7CDC7 CDC16 CDC20 DKC1 CDCA7L CDC45 CDC25C CDC25B DNAJB6 CEP57 CDCA5CDCA2 CDC27 DSP CHAF1A CDKN2AIP CDCA3 CDC42EP1 DYNLL1 CHAF1B CENPM CDCA8CDCA3 EIF4E CLSPN CENPQ CDK1 CENPA ELP3 CREBZF CERS6 CDKN1B CENPE FAM60ACTSD CHML CDKN2C CENPF FAM189B DIS3 COQ9 CDR2 CEP55 FOPNL DNAJC3 CPNE8CENPL CFLAR FOXK2 DONSON CREBZF CEP350 CIT FXR1 DSCC1 CRLS1 CFD CKAP2G3BP1 DTL DCAF16 CFLAR CKAP5 GATA2 E2F1 DEPDC7 CHEK2 CKS1B GNB1 EIF2ADHFR CKAP2 CKS2 GRPEL1 ESD DNA2 CKAP2L CNOT10 GSPT1 FAM105B DNAJB4 CYTH2CNTROB GTF3C4 FAM122A DONSON DCAF7 CTCF HIF1A FLAD1 DSCC1 DHX8 CTNNA1HMG20B GINS2 DYNC1LI2 DNAJB1 CTNND1 HMGCR GINS3 E2F8 ENTPD5 DEPDC1HSD17B11 GMNN EIF4EBP2 ESPL1 DEPDC1B HSPA8 HELLS ENOSF1 FADD DIAPH3 ILF2HOXB4 ESCO2 FAM83D DLGAP5 JMJD1C HRAS EXO1 FAN1 DNAJA1 KDM5B HSF2 EZH2FANCD2 DNAJB1 KIAA0586 INSR FAM178A G2E3 DR1 KIF5B INTS8 FANCA GABPB1DZIP3 KPNB1 IVNS1ABP FANCI GAS1 E2F5 KRAS KIAA1147 FEN1 GAS2L3 ECT2LARP1 KIAA1586 GCLM H2AFX FAM64A LARP7 LNPEP GOLGA8A HAUS8 FOXM1 LRIF1LUC7L3 GOLGA8B HINT3 FYN LYAR MCM2 H1F0 HIPK2 G2E3 MORF4L2 MCM4 HELLSHJURP GADD45A MRPL19 MCM5 HIST1H2AC HMGB2 GAS2L3 MRPS2 MCM6 HIST1H4C HN1GOT1 MRPS18B MDM1 INTS7 HP1BP3 GRK6 MSL1 MED31 KAT2A HRSP12 GTSE1 MTPNMRI1 KAT2B IFNAR1 HCFC1 NCOA3 MSH2 KDELC1 IQGAP3 HMG20B NFIA NASPKIAA1598 KATNA1 HMGB3 NFIC NEAT1 LMO4 KCTD9 HMMR NUCKS1 NKTR LYRM7 KDM4AHN1 NUFIP2 NPAT MAN1A2 KIAA1524 HP1BP3 NUP37 NUP43 MAP3K2 KIF5B HPS4ODF2 ORC1 MASTL KIF11 HS2ST1 OPN3 OSBPL6 MBD4 KIF20B HSPA8 PAK1IP1 PANK2MCM8 KIF22 HSPA13 PBK PCDH7 MLF1IP KIF23 INADL PCF11 PCNA MYCBP2 KIFC1KIF2C PLIN3 PLCXD1 NAB1 KLF6 KIF5B PPP2CA PMS1 NEAT1 KPNA2 KIF14 PPP2R2APNN NFE2L2 LBR KIF20B PPP6R3 POLD3 NRD1 LIX1L KLF9 PRC1 RAB23 NSUN3LMNB1 LBR PSEN1 RECQL4 NT5DC1 MAD2L1 LMNA PTMS RMI2 NUP160 MALAT1 MCM4PTTG1 RNF113A OGT MELK MDC1 RAD21 RNPC3 ORC3 MGAT2 MIS18BP1 RAN SEC62OSGIN2 MID1 MKI67 RHEB SKP2 PHIP MIS18BP1 MLLT4 RPL13A SLBP PHTF1 MND1MZT1 SLC39A10 SLC25A36 PHTF2 NCAPD3 NCAPD2 SNUPN SNHG10 PKMYT1 NCAPHNCOA5 SRSF3 SRSF7 POLA1 NCOA5 NEK2 STAG1 SSR3 PRIM1 NDC80 NUF2 SYNCRIPTAF15 PTAR1 NEIL3 NUP35 TAF9 TIPIN RAD18 NFIC NUP98 TCERG1 TOPBP1 RAD51NIPBL NUSAP1 TLE3 TRA2A RAD51AP1 NMB ODF2 TMEM138 TTC14 RBBP8 NR3C1ORAOV1 TOB2 UBR7 REEP1 NUCKS1 PBK TOP1 UHRF1 RFC2 NUMA1 PCF11 TROAP UNGRHOBTB3 NUSAP1 PLK1 TSC22D1 USP53 RMI1 PIF1 POC1A TULP4 VPS72 RPA2PKNOX1 POM121 UBE2D3 WDR76 RRM1 POLQ PPP1R10 VANGL1 ZMYND19 RRM2 PPP1R2PRPSAP1 VCL ZNF367 RSRC2 PSMD11 PRR11 WIPF2 ZRANB2 SAP30BP PSRC1 PSMG3WWC1 SLC38A2 RANGAP1 PTP4A1 YY1 SP1 RCCD1 PTPN9 ZBTB7A SRSF5 RDH11 PWP1ZCCHC10 SVIP RNF141 QRICH1 ZNF24 TOP2A SAP30 RAD51C ZNF281 TTC31 SKA3RANGAP1 ZNF593 TTLL7 SMC4 RBM8A TYMS STAT1 RCAN1 UBE2T STIL RERE UBL3STK17B RNF126 USP1 SUCLG2 RNF141 ZBED5 TFAP2A RNPS1 ZWINT TIMP1 RRP1TMEM99 SEPHS1 TMPO SETD8 TNPO2 SFPQ TOP2A SGOL2 TRAIP SHCBP1 TRIM59SMARCB1 TRMT2A SMARCD1 TTF2 SPAG5 TUBA1A SPTBN1 TUBB SRF TUBB2A SRSF3TUBB4B SS18 TUBD1 SUV420H1 UACA TACC3 UBE2C THRAP3 VPS25 TLE3 VTA1TMEM138 WSB1 TNPO1 ZNF587 TOMM34 ZNHIT2 TPX2 TRIP13 TSG101 TSN TTKTUBB4B TXNDC9 TXNRD1 UBE2D3 USP13 USP16 VANGL1 WIBG WSB1 YWHAH ZC3HC1ZFX ZMYM1 ZNF207

TABLE 4 List of cell cycle regulated genes identified from the analysisof 589 HEK and 412 3T3 cells. Intersection human novel gene clustermouse gene All genes genes annotation CCNE2 1 Shmt1 CDC6 1 Zmym1 ACTBACTB CLSPN 1 Meaf6 AKIRIN2 ARHGAP11A DTL 1 Usp37 ANLN ARL6IP6 MCM3 1Msh6 ANP32E ARPC2 MCM5 1 Rbbp4 ARHGAP11A ATF4 TF MCM6 1 Bri3bp ARL6IP1CCAR1 MSH6 1 Rrp8 ARL6IP6 CCDC18 PCNA 1 Mb21d1 ARPC2 CDCA4 CC UNG 1Wdhd1 ASF1B DNAJC9 ADAMTS1 1 Mcm5 ASPM DNMT1 ARL6IP6 1 Smarca5 ATAD2E2F7 TF/CC ATAD2 1 Slc1a5 ATF4 FTH1 BLM 1 Nap1l4 AURKA GOLGA2 C4orf21 1Nolc1 AURKB GPSM2 CASP8AP2 1 D10Wsu102e BIRC5 H3F3B CC CCNE1 1 Ckap4 BLMHIST1H1E CC CDCA7 1 Timeless BORA MBNL1 CHAF1A 1 Zfp367 BRD8 MCMBP CCCHAF1B 1 Zmynd19 BRIP1 MRPL17 E2F1 1 Cdc25a BUB1 NCAPG CC E2F8 1 Atp2b1BUB1B NDUFA1 FEN1 1 Smarcc1 BUB3 NXT1 GINS2 1 Ccnd2 CALM2 OSBPL8 1 LbhCASC5 OTUB1 HIST1H2BK MCM2 1 Maff CASP8AP2 PARPBP CC MCM7 1 Casp3 CBX5PRRC2C MCM10 1 Tnfaip8 CCAR1 RPL26 MCMBP 1 Amotl1 CCDC18 SNHG3 MMS22L 1Rfc1 CCNA2 SRP9 PKMYT1 1 Cdc42ep3 CCNB1 TCF19 TF PRIM1 1 Gpr180 CCNB2TK1 RAD51 1 Oaf CCNE1 TUBA1C RFC4 1 Gins3 CCNE2 UBC SLBP 1 Cdc7 CCNFWDHD1 SNHG3 1 Cactin CDC6 ZFHX4 TF TIPIN 1 Eps8 CDC20 TK1 1 Slk CDC27TMEM97 1 Smc3 CDC45 UHRF1 1 Alad CDCA2 WDR76 1 Nasp CDCA3 XRCC2 1 Smc5CDCA4 ZMYND19 1 Fen1 CDCA7 ZNF367 1 Ctnnal1 CDCA8 CDC45 1 Enkd1 CDK1DNAJC9 1 Tjp2 CDK5RAP2 DSCC1 1 Nup43 CDKN1B DUT 1 Dek CDKN2C EXO1 1 SlbpCENPA FBXO5 1 Ung CENPE H1F0 1 Paics CENPF HELLS 1 Gins2 CEP55 HIST1H4C1 Umps CHAF1A HSPB11 1 Pdlim1 CHAF1B IRS4 1 Gart CKAP2 KIAA0101 1 Whsc1CKAP2L MCM4 1 Baz1b CKAP5 MLF1IP 1 Efnb2 CKS1B MSH2 1 Pola2 CLSPN POLD31 Ivns1abp CTCF PSMC3IP 1 Dnaaf2 DBF4 RAD51AP1 1 Trmt2a DLGAP5 RRM2 1E2f1 DNAJC9 TCF19 1 Chaf1b DNMT1 TYMS 1 Syngr2 DSCC1 UBE2T 1 Mcmbp DTLACAA1 1 Cdt1 E2F1 ACYP1 1 Pold3 E2F7 ALDOA 1 Ubr7 E2F8 ARID3A 1 Grsf1ECT2 ARPC2 1 Dck ERCC6L ARPC5 1 Atad5 ESPL1 ASF1B 1 Casp8ap2 EXO1 ASRGL11 Orc2 FAM64A ATP5E 1 Siva1 FAM83D ATP6V1D 1 Cdca7 FBXO5 ATP6V1F 1 Rif1FEN1 ATP6V0E2 1 Ptrh2 FOXM1 B2M 1 Arl6ip6 FTH1 BRIP1 1 Rnf168 G2E3C1orf21 1 Tfrc GAS2L3 C3orf14 1 Fancl GINS2 C4orf48 2 Clspn GMNN C5orf222 Lig1 GOLGA2 C19orf53 2 Gmnn GPSM2 C21orf58 2 Dtl GTSE1 CALM1 2 Uhrf1H1F0 CAMTA1 2 Ccne1 H3F3B CARHSP1 2 Fam111a HAT1 CCDC51 2 Tcf19 HELLSCDCA4 2 Dnmt1 HEXIM1 CLTB 2 Msh2 HIST1H1E COX6B1 2 Orc6 HJURP COX7C 2Mcm6 HMGB2 COX8A 2 Pcna-ps2 HMMR COX17 2 Mcm2 HN1 DDX46 2 Hells HP1BP3DGCR8 2 Haus6 INCENP DMC1 2 Ccne2 KDM5B DNMT1 2 Ppat KIF2C DONSON 2Dscc1 KIF11 DTYMK 2 Cdc6 KIF14 E2F7 2 Rpa2 KIF15 ERCC6L 2 Atad2 KIF18AFADS1 2 Mcm3 KIF20A FAM178A 2 Pcna KIF20B FANCA 2 Mcm7 KIF23 FAU 2Chaf1a KIFC1 FTH1 2 Hat1 LIG1 FTL 2 Rrm2 LUC7L3 GAPDH 2 Slfn9 MALAT1GGCT 2 Rfc3 MBNL1 GMNN 2 Mcm4 MCM2 H2AFZ 3 Ldlr MCM3 HAUS1 3 Amotl2 MCM4HAUS5 3 Topbp1 MCM5 HOMEZ 3 Ncapd3 MCM6 LAGE3 3 Haus8 MCM7 LIG1 3 Rbl1MCM10 MED31 3 Rrm1 MCMBP MGST3 3 Elovl5 MED31 MRPL17 3 Dhfr MELK MSANTD33 Usp1 MIS18BP1 MYBL2 3 Ncapg2 MKI67 MYL6 3 Asf1b MLF1IP NASP 3 Dcaf15MRPL17 NDUFA1 3 Tssc4 MSH2 NDUFB1 3 Hjurp MSH6 NDUFB2 3 Hist1h2ak NASPNDUFS5 3 Nup155 NCAPD2 NPAT 3 Skp2 NCAPG NPC2 3 Tdp2 NCAPH NXT1 3 Cbx5NDC80 OPTN 3 Hspa14 NDUFA1 ORC6 3 Mcm10 NEK2 PGK1 3 Prim1 NUF2 PHTF1 3Exo1 NUSAP1 PIGX 3 Apbb1ip NXT1 PLSCR1 3 Eri1 ODF2 POLA1 3 Smchd1 ORC6POLR2H 3 Dnajc9 OSBPL8 POU4F1 3 Akap11 OTUB1 PPDPF 3 Mlf1ip PARPBP RABIF3 Tyms PCNA RFC2 3 Nfx1 PCNT RNASEH2A 3 E2f7 PKNOX1 RNASEH2C 3 Ubap2PLK1 RPA3 3 Chtf18 POLA1 RPS5 3 Stub1 POLD3 RRM1 3 Esco2 PPP2R5C S100A103 Ezh2 PRC1 SEMA3C 3 Pold1 PRIM1 SERF2 3 Apbb2 PRR11 SHFM1 3 E2f8 PRRC2CSLC25A4 3 Cyp51 PSRC1 SLC25A5 3 Rad54l PTTG1 SNHG1 3 Nxt1 RACGAP1 SNHG93 Pola1 RAD51 SNRPD2 3 Rpa3 RAD51AP1 SNX10 3 Fbxo5 RANGAP1 SRP9 3 Il1rl1RBBP6 SS18L2 3 Fhl2 RFC2 SSR4 3 Mis18a RFC4 STMN1 3 Tex30 RPA3 SVIP 3Idh2 RPL26 TCEB1 3 Mybl1 RRM1 TIMP1 3 Prkca RRM2 TM7SF2 3 Rer1 SGOL1TMSB10 3 Blm SGOL2 TOPBP1 3 Rpa1 SKA2 TPM4 3 Pole SLBP TTLL7 3 Rfc2 SMC4TUBA1A 3 Mtbp SNHG3 UBA52 3 Nup107 SPAG5 UBR7 3 Sqle SPC25 USMG5 3 CenphSRP9 USP1 3 Plk4 TACC3 WDHD1 3 Apitd1 TCF19 YBEY 3 Lrr1 TIPIN ZNF260 3Haus3 TK1 ZNF428 3 Slc25a1 TMPO ZNF711 3 Acat2 TOP2A ZNF720 3 Sc4molTOPBP1 ACTB 3 Smc6 TPX2 AIG1 3 Cdca5 TRIM59 ANKRD36C 3 Tk1 TTK ANXA5 3Thbs1 TUBA1C ARL13B 3 Cdc45 TUBB4B BAD 3 Cyr61 TYMS BUB3 3 Brca1 UACAC2orf68 3 Lphn2 UBC C19orf43 3 Rad51 UBE2C CBX5 3 Rad51ap1 UBE2T CCDC143 Rbmx2 UBR7 CCNL2 3 Nup85 UHRF1 CDADC1 3 Pradc1 UNG CDK1 3 Tipin USP1CDKN2C 3 Rad18 WDHD1 CIRBP 3 Ankrd1 ZFHX4 CREB5 3 Fignl1 ZMYM1 DBF4B 3Tanc2 ZMYND19 DDX17 3 Rfc4 DPP9 3 Brip1 DUSP3 3 Etaa1 ELF1 3 Slc7a1FAM76A 3 Ank3 FAM126A 4 Cdca8 FAM192A 4 Ncapg FANCD2 4 Nuf2 FKBP2 4Gas2l3 FOXC1 4 Ndc80 FOXM1 4 Pbk GATAD2B 4 Cdkn1b GNPTAB 4 Cdkn2cGOLGA8B 4 G2e3 GPX4 4 Smc2 GTPBP3 4 Tuba1c HIST1H1C 4 Racgap1 HIST1H1E 4Kif11 HIST2H2AC 4 Incenp HJURP 4 Cep55 HOXA3 4 Dbf4 HOXA10 4 Kif2c HOXB74 Fam83d IGF2BP2 4 Ccna2 ING3 4 Prc1 IQGAP3 4 Hmgb2 JUN 4 Aurkb KIAA15244 Top2a KIFC1 4 Kif22 LARP7 4 Shcbp1 LRRC49 4 Ect2 MAF 4 Mis18bp1 MED214 Spc25 MELK 4 Kif4 N4BP2L2 4 Ccnf NMT2 4 Cenpl NT5C 4 Sgol1 OSBPL3 4Sgol2 OTUB1 4 Casc5 PERP 4 Mki67 RAB5B 4 Fam64a RBM23 4 Kif20b RBMS1 4H1f0 ROCK1 4 Smc4 SCP2 4 Kif15 SKA2 4 Prr11 SP3 4 Cdk1 SRSF5 5 FliiTFAP2A 5 Adprhl2 THG1L 5 Col6a1 TIMM17B 5 Ubc TMPO 5 Mcph1 TROAP 5Col16a1 TSC22D3 5 Cenpn TSIX 5 Trip13 TUBB 5 Mrpl17 TUBGCP3 5 Parva UBA55 Myadm UBC 5 Ercc6l XIST 5 Arhgef40 XXYLT1 5 Pdgfrb YWHAB 5 Cd81 ZNF5035 Ska1 ZNF503- 5 Hist1h1e AS2 ZNF703 5 Ccdc53 ZWINT 5 Espl1 AASDH 5 AaasAKIRIN2 5 Sp1 ANKRD11 5 Mad2l1 APC 5 Rsu1 ARHGAP11A 5 Cryab ARID2 5Egln2 ASH1L 5 Tmpo ATF4 5 Mastl ATL2 5 Ephx1 BEX1 5 Tpgs2 BOD1L1 5Lclat1 BORA 5 Rhno1 BTAF1 5 Foxm1 C6orf62 5 Atf4 C10orf118 5 BC003965CARD8 5 Osbpl8 CASC5 5 Lmnb1 CCDC18 5 Fez2 CCDC88A 5 Ndufv1 CCNA2 5Osbpl9 CCNB2 5 Otub1 CCNF 5 Atxn10 CDC27 5 Gtse1 CDCA2 5 Fam173a CDKN1B5 Gemin6 CENPA 5 Bgn CENPI 5 Rfc5 CEP44 5 Malat1 CEP350 5 Fer CKAP2 5Ncaph2 CKAP2L 5 Meg3 CKS1B 5 Cdca2 CLCN3 5 Stil COASY 5 Pcnt CSNK1G3 5Tubb5 CTCF 5 Mdc1 DCP1A 5 Cuta DEPDC1B 5 Tuba1b DIAPH2 5 Cst3 DR1 5Slc35f5 DSC3 5 Ttk DST 5 Tsen2 EIF1B 5 Raf1 EIF4G3 5 Urod ESPL1 5 Ttf2FAM64A 5 Srgap2 FAM83D 5 Ndufa1 GAS2L3 5 Ubb GOLGA4 5 Cntln GPSM2 5 CtcfGTPBP6 5 Fra10ac1 HMGB2 5 Pmp22 HN1 5 Thsd7a HP1BP3 5 Angptl2 ICT1 5Ube2t INO80D 5 Pknox1 ITSN2 5 Cxcl12 KDM5B 5 Vamp5 KIAA0586 5 Ercc5KIF2C 5 Kif18a KIF4B 5 Ebag9 KIF5B 5 Sap30 KIF15 5 Ska3 MALAT1 5 Ccdc34MAP9 5 Atp6v1g1 MSX2 5 Fbln2 MT-ND5 5 Cenpq MT-RNR1 5 Adat2 MT-RNR2 5Dlk1 NCAPD2 5 Lsm3 NCOA2 5 Xiap NEK2 5 Hirip3 NUSAP1 5 Stag2 OSBPL8 5Skiv2l PBRM1 5 Cenpc1 PCLO 5 Hcfc1r1 PDZD8 5 Cdk5rap2 PHACTR4 5 Stx4aPHF20L1 5 Gen1 PPP1R12A 5 Fam3c PRR11 5 Uaca PTBP3 5 Chrac1 PTPN1 5Pcif1 RACGAP1 5 Ing1 RANGAP1 5 Add1 RC3H1 5 Gabarap RICTOR 5 Rnf24 RUFY15 Zrsr2 SAFB 5 Tbk1 SERTAD2 5 Lsm2 SGOL1 5 Dbnl SMC4 5 Smoc2 SPAG5 5Puf60 SPG11 5 Ppp1r35 SRRM2 5 Bub3 TAF3 5 Melk THUMPD1 5 Kifc1 TJP1 5Dock1 TLE3 5 Gabpb1 TRIO 5 Zwilch TUBA1C 5 Mbnl1 TUBB4B 5 Grn UACA 5Med31 UBE2D1 5 Ncaph UBLCP1 5 Ifit2 USP9X 5 Id2 VPS13A 5 Cdca4 WAC 5Ddx49 WDR36 5 Cope WDR53 5 Gsg2 YTHDC1 5 Sass6 ZC3H4 5 Arf2 ZCCHC11 5Nfu1 ZFR 5 Id3 ZIC5 5 Apip ZMAT2 5 H3f3b ZMYM1 5 Cat ZMYND8 5 Trim59ZNF280D 5 Lpp ZNF281 5 Dcaf7 ZNF638 5 Rasl11a ZNF652 5 Rtkn2 ZYG11B 5Ska2 ANLN 5 Bicc1 ARL6IP1 5 Golga2 ASPM 5 Col1a1 AURKA 6 Anln AURKB 6Kif20a BIRC5 6 Cenpf BRD8 6 Ckap2 BUB1 6 Cenpa BUB1B 6 Bub1 CCNB1 6 HmmrCDC20 6 Ckap2l CDCA3 6 Aurka CDCA8 6 Pttg1 CENPE 6 Plk1 CENPF 6 CenpeCKAP5 6 Tacc3 CKS2 6 Tpx2 DBF4 6 Tubb4b DEPDC1 6 Cdc20 DLGAP5 6 AspmECT2 6 Ccnb1 G2E3 6 Ckap5 GTSE1 6 Ube2c HMMR 6 Arhgap11a INCENP 6 Birc5KIF11 6 Kif23 KIF14 6 Nusap1 KIF18A 7 Serpinb8 KIF20A 7 Gm10184 KIF20B 7Gas5 KIF23 7 Dnm3os KPNA2 7 Chchd7 MKI67 7 Cstb NCAPG 7 Smtn NDC80 7Fam172a NUF2 7 Cdkn3 PIF1 7 Dlgap5 PLK1 7 Mgea5 PRC1 7 Opa3 PSRC1 7Tax1bp1 SGOL2 7 Parpbp TACC3 7 Nup37 TOP2A 7 Gas1 TPX2 7 Grem2 TTK 7Uhrf1bp1l UBE2C 7 Ccnb2 ABCC5 7 Brd8 ABI1 7 Cdc25c ACIN1 7 Nek2 ANP32E 7Cmas ARFGEF2 7 Mrps16 ARHGAP5 7 Hyls1 ARHGAP12 7 Stk11 ARHGAP19 7 Diap3ARIH1 7 Bora ATF7IP 7 Cit BPGM 7 Rangap1 C10orf32 7 Tm7sf3 C11orf54 7Arl2bp CALM2 7 Elp3 CAMLG 7 Map2k2 CCAR1 7 Specc1l CCNJ 7 H2afx CDK5RAP27 Smarcb1 CEP70 7 Rad23a COMMD2 7 Fzr1 CREBRF 7 Rfk CTNND1 7 Bax CUL5 7Cdkn2d DCP2 7 Rhoq DDX21 7 Ccdc77 DESI2 7 Tgif1 DHX36 7 Calm2 DHX37 7Rpl13a-ps1 EP300 7 Reep4 EVI5 7 Ccdc18 EXPH5 7 Itfg1 FASTKD1 7 Lhfpl2GAPVD1 7 Zfhx4 GOT1 7 Arl6ip1 H3F3B 7 Zbed3 HEXIM1 7 Rab7 HMGB3 7 Nucks1HMGCR 7 Fam198b HSPA1B 7 Nfe2l1 HSPA5 7 Mat2b HSPH1 7 Tmem138 KIF4A 7Ccng2 LARP4B 7 Ccng1 LBR 7 Chd2 LIX1L 7 Armcx1 LRIF1 7 Cep128 LUC7L3 7Dnajc10 MARK2 7 E2f5 MBNL1 7 Chchd6 MIS18BP1 7 Fgfr1op MT-ND1 7 Ppa2MT-ND2 7 Rbbp6 MT-ND4 7 Acot9 MT-ND4L 7 Rhou MTRNR2L8 7 Rad21 MTRNR2L127 Kif14 NFKB1 7 Asxl1 NIPBL 7 Cep110 ODF2 7 Ppp2r5c PARPBP 7 Mesdc2 PCM17 Pdha1 PCNT 7 Mapre1 PDE6D 7 Gja1 PICALM 7 Zfand6 POLR2B 7 Cdca3 PRRC2C7 Terf1 PTPN13 7 Rbms3 PTTG1 7 Slc7a5 PUM1 7 Cpne3 RAB7L1 7 Ptms RAB14 7Cdc25b RB1CC1 7 Pcf11 RBBP6 7 Ddit4 RBMX 7 Carkd RNF26 7 Ndufc1 RRP15 7Ncapd2 RSF1 7 Mrpl51 SAPCD2 7 Bola3 SATB2 7 Uhrf2 SEC62 7 Bub1b SENP6 7Golga5 SESN2 7 Spag5 SETD2 7 Trappc2l SF1 7 Psrc1 SFPQ 7 Dynll1 SLC7A117 Vbp1 SLC39A10 7 Gpsm2 SMEK2 7 Ubxn6 SNAPC3 7 Dnajb4 SON 7 Glrx3 SRSF37 Sar1a STX18 7 Cenpw TAF7 7 Hn1 TFCP2 7 Odf2 TGS1 7 Atg3 TMEM19 7 Echs1TOX4 7 Fzd2 UBXN4 7 Arl8b UNKL 7 Hexim1 USP7 7 Pnrc2 VEZF1 7 Atp6ap2WBP11 7 Cks1b WDR43 7 Unc50 WSB1 7 Akirin2 ZC3H11A 7 Cebpb ZC3H14 7C330027C09Rik ZNF148 7 Cdc27 ZNF318 7 Cd164 7 F3 7 Pcnp 7 Hp1bp3 7 Nde17 Ccdc104 8 Arpc2 8 Snhg3 8 Marcksl1 8 Dhx29 8 Sbno1 8 Dnajc19 8 Socs4 8Hnrnpc 8 Rps14 8 Gltscr2 8 Ncl 8 Csnk1a1 8 Ercc1 8 Oraov1 8 Ccnd1 8Myeov2 8 Rala 8 Itga5 8 Serbp1 8 Naca 8 Vim 8 Impact 8 Hnrnpu 8 Snrpa 8Sox4 8 Pycr2 8 Celf4 8 Srp9 8 Sltm 8 Hspa9 8 Rpl15 8 Pus3 8 Tsc22d1 8Mrpl21 8 St13 8 Cwc15 8 Gpx7 8 Dhx38 8 Hspb8 8 Timm13 8 Rnf11 8 Snrpd3 8Arl3 8 Zfp36l2 8 Strap 8 Ddx6 8 Eif2s1 8 Nrbp1 8 Hsp90ab1 8 Zfp36l1 8Pdcd4 8 Hmgn3 8 Atp5j 8 Ikbkap 8 Tbca 8 Npm1 8 Fth1 8 Banf1 8 Psmc5 8Hspa4 8 Slc41a1 8 Rpl32 8 Cct8 8 S100a6 8 Gm6563 8 Top1 8 Syncrip 8Zfc3h1 8 Kdm5b 8 Mrpl38 8 Rps24 8 Gm4204 8 Tes 8 Rpl26 8 Nol8 8 Arf4 8Tardbp 8 Gnb2l1 8 Nrf1 8 Hsp90aa1 8 Hdgf 8 Stat3 8 Zbtb38 8 Hmga2 8Nufip2 8 Sh3glb1 8 Irf2bp2 8 Sqstm1 8 Canx 8 Rps21 8 Exo5 8 Ubtd1 8Hspd1 8 Anp32e 8 Lmna 8 Ogfr 8 Rps3 8 Mex3a 8 Mpp1 8 Pfn1 8 Prrc2c 8Crlf3 8 Ubtf 8 Bzw1 8 Rpl4 8 Lgals1 8 Actb 8 Ccar1 8 Adar 8 Ddx3x 8 Tlk28 Dcun1d5 8 Luzp1 8 Tomm70a 8 Ccdc6 8 Luc7l3 8 Gm9843 8 Rsl1d1 8 Rtn4

TABLE 5 List of highest gene loadings in each of the top 40 principalcomponents from the 44,808 retina STAMPs. Top and bottom genes PC1 PC2PC3 PC4 PC5 PC6 PC7 PC8 PC9 PC10 1 CP ATP1B1 ISL1 PDE6H PRKCA EBF3 SNCGTHY1 CBLN2 SLIT2 2 CAR14 SNHG11 TRPM1 ARR3 CCDC136 SLC6A9 NRN1 SLC17A6C1QL1 TACR3 3 SLC1A3 PAX6 GNG13 GUCA1A KCNE2 LGR5 SLC17A6 NRN1 IGFBP2NXPH1 4 APOE ELAVL3 VSX2 PDE6C ABLIM1 EBF1 NEFM NELL2 C1QL2 PDE1A 5 CD9SLC6A1 SCG2 GNAT2 CAR8 PRDM13 MEFL LPL OLFM3 GLRA1 6 COL9A1 GAD1 GPR179OPN1MW SEBOX ZFP804A FXYD7 TFAP2C TBX3 NETO1 7 RLBP1 VSNL1 PCP2 GNGT2VSTM2B NFIX RGS4 BHLHE22 GNG2 NTNG1 8 AQP4 STMN2 GRM6 OPN1SW STRIP2PTPRF NELL2 NPNT CARTPT CDH8 9 ID3 SPOCK3 QPCT RP1 PDE6H PTPRT STMN2CPLX2 GAP43 ZFHX4 10 SPC25 GAD2 TRNP1 GNB1 ARR3 NEFL CHRNA6 FXYD7 NFIAA330008L17RIK 11 PDPN SPARCL1 NDNF KCNE2 PDE6C NHLH2 THY1 AI593442 MEIS2TMEFF2 12 CRYM CPLX2 CAR8 THRB OPNIMW LAMP5 RPRM MAF NR4A2 ESAM 13ABCA8A CDK14 B3GALT2 CNGB3 PCP2 CALB2 ELAVL2 RGS4 COL11A1 PRDM8 14 TIMP3TFAP2B TGFB2 CST3 LRRTM4 PPP1R17 UCHL1 ALCAM SYT7 SLITRK6 15 HES1 DLGAP1PRKCA FAM19A3 CEP112 CRABP1 GAP43 CXCL14 2610017I09RIK CACNA2D3 16 CYR61C1QL1 DKK3 CD59A TP8G SNCG NEFH NECAB1 TFAP2B BHLHE22 17 ZFP36L1 GNG2FRMD3 MFGE8 ZBTB20 NCKAP5 FSTL1 GAD2 OPTC A730046J19RIK 18 GPR37 TKTSIX3OS1 HOPX ADAMTS5 IER5 KCNIP4 PTN VIP SEBOX 19 SPARC DNER CACNA2D3BTG2 OPN1SW NEFM CALB2 CRABP1 COL23A1 QPCT 20 ESPN RBFOX1 PAX6 HSPA1AGUCA1A HS6ST2 CDK14 ELAVL2 SLC4A3 GRIK1 −1 SNHG11 GNG13 CLDN5 ABLIM1SCGN GAD1 NHLH2 1500016L03RIK SLC5A7 CDH9 −2 SCG2 TRPM1 ELTD1 ISL1A730046J19RIK SLC6A1 SLC6A9 CALB1 GNG7 HS3ST4 −3 ATP1B1 PCP2 CD93 PCP2CDH8 ID4 NECAB1 TMEFF2 RIMS1 RELN −4 UCHL1 GPR179 PTPRB TRPM1 VSX1 NPNTCRABP1 BAI1 CALB2 NFIA −5 ELAVL3 GRM6 CTLA2A CAR8 PTPRZ1 C1QL2 TFAP2CSLC4A3 NPY PTPRZ1 −6 SPOCK3 ISL1 PLTP GPR179 GSG1 LPL LGR5 SEPT4 CXCL14BC046251 −7 GABRA1 VSX2 LY6C1 TGFB2 SLIT2 MEIS2 LAMP5 TFAP2B RBFOX1SLC5A7 −8 VSNL1 TRNP1 RAMP2 PRKCA ZFHX4 C1QL1 PRDM13 SOWAHA IGFBP7 EPHA7−9 STMN2 CAR8 FAM101B GNG13 GRIK1 SLIT2 NFIX SGK1 NHLH2 SOX6 −10 GAD1QPCT MGP QPCT PDE1A PCP4L1 IER5 TPM3 PCP4L1 RIMS1 −11 ISL1 FRMD3 RGS5SPARCL1 NETO1 GAD2 ZFP804A VIM SOX2 NEUROD2 −12 GNG13 SEBOX EGFL7 VSTM2BGABRA1 ZFHX4 PTPRF NPY SCG2 CHODL −13 TRNP1 NDNF GNG11 TRNP1 TACR3DLGAP1 NCKAP5 TPM3-RS7 ARL4C GNG7 −14 RBFOX1 CACNA2D3 IGFBP7 VSX2SLITRK6 CXCL14 GRIK2 NEBL PCDH10 GJD2 −15 TFAP2B B3GALT2 SEPP1 GRM6A330008L17RIK CBLN2 FILIP1L SLC5A7 POMC GABRR2 −16 B3GALT2 STRIP2 VWA1COL4A1 NXPH1 ALDOC PTPRT NEFH SPOCK3 ISL1 −17 CPLX2 TGFB2 ITM2A CACNA2D3OTOR RND3 EBF3 GNG7 SPARCL1 COL1A2 −18 FRMD3 GABRR2 COL4A1 COL4A2 CAMK4SPOCK3 GAD2 C1QL1 ESPN GRM6 −19 GNG2 PRKCA SLC7A5 NDNF ESAM FILIP1LBHLHE22 ZFP804A LPL NDNF −20 PCP4L1 RNF152 FN1 B3GALT2 FEZF2 SCGN NR2F2FBXW7 CALB1 IGFN1 Top and bottom genes PC11 PC12 PC13 PC14 PC15 PC16PC17 PC18 PC19 PC20 PC21 1 FOSB CARTPT OPTC VSX1 GNB1 CCK OLFM3 CBLN2CARTPT OPTC IGF1 2 ZFP36 2610017I09RIK GNB1 RELN RP1 OTOR CAR2 NETO1NR4A2 ALDH1A1 IGFN1 3 JUNB TFAP2B CST3 CCK CST3 LECT1 LAMP5 SYT6 LRRTM1ITM2A TFAP2C 4 EGR1 NR4A2 RP1 LECT1 SLC16A1 UNC13C GJD2 CDH9 NFIA SNED1LAMP5 5 FOS GABRA2 ATP1A2 PCP4L1 HS3ST4 CABP2 DYNC1I1 TACR3 VIP SNCACARTPT 6 ATF3 CBLN2 SNED1 CDHB S1PR1 GSG1 SLC6A9 NPY RPRM TAC2 CABP2 7NR4A1 FBXW7 IGFBP2 TNNT1 KCNJ10 COL11A1 GRIA3 HS3ST4 SCG2 PVRL3 PCDH17 8DUSP1 VIP MEST IGF1 CDH9 C1QL1 TBX3 NFIX 2610017I09RIK LY6E PTPRF 9 IER2SYT6 FSTL1 IGFN1 ABCA8A SCGN AI593442 NXPH1 LHX4 PTGDS NR2F2 10 KLF4HPGD IGF2 ZFHX4 BC046251 NHLH2 PTPRF RIMS1 EPHA7 CLDN5 NR4A2 11 PPP1R15ASLC5A7 CDKN1C SCG2 NEUROD2 RELN IGFBP2 COL11A1 NFIX MEST FN1 12 KLF6NNAT HTRA1 A330008L17RIK WIPI1 TFAP2C THY1 PDE1A GPR22 CTLA2A HS3ST4 13BTG2 GAD1 PTGDS SIX3OS1 LY6C1 CST3 NEFH C1QL1 TNNT1 IGFBP2 HTRA1 14CYR61 GRIA3 NXPH1 GJD2 ABCA8B GNB1 DLGAP1 NHLH2 PTPRZ1 RAMP2 SLC6A9 15NFKBIZ SCG2 WLS RPRM CLDN5 RP1 ABLIM1 GAP43 HS6ST2 VWA1 HS6ST2 16 RP1GRIK2 PVRL3 UNC13C SPC25 CRABP1 BC046251 GNG7 BHLHE22 LY6C1 SLC17A8 17GNB1 RIMS1 HSPA1A GJC1 KDR NFIB CNTN4 TBX3 TFAP2C CTSH COL11A1 18 JUNCALB2 SGK1 GNGT2 HSPA1B EBF3 FILIP1L NR2F2 ISL1 SLC7A5 OPTC 19 GM26669KCND3 HSPA1B LAMP5 NETO1 TBX3 CDKN1C NR4A2 NECAB1 TAC1 NECAB1 20 ADAMTS1CAR2 ALDH1A1 GNG13 CAV1 A730046I19RIK RBFOX1 CHODL SOX6 PPP1R172610017I09RIK −1 OPTC 1500016L03RIK GNGT2 GSG1 OPTC NEUROD22610017I09RIK HPGD IGFN1 MGP PPP1R17 −2 CD59A LPL GNAT2 OTOR ATP1A2NXPH1 KCND3 FBXW7 PCDH17 RGS5 IGFBP5 −3 GNAT2 BHLHE22 FAM19A3 GRIK1FSTL1 BC046251 IGFBP5 2610017I09RIK IGFBP5 GJC1 SNCA −4 GNGT2 MAF GSG1FEZF2 IGFBP2 LAMP5 IGFN1 LECT1 IGFBP2 SERPINE2 LECT1 −5 PDE6C CXCL14LHX4 NNAT ALDH1A1 NFIA NR4A2 UNC13C FN1 CALD1 CCK −6 OPN1MW TFAP2C PDE6CLHX4 ZFP36 NETO1 GRIK2 DNER PPP1R17 RGS4 RGS5 −7 ARR3 NPNT ARR3 SLITRK6SNED1 TACR3 GABRA2 LAMP5 OLFM3 COL1A2 EBF1 −8 ATP1A2 CPLX2 OPN1MW KCNIP4PTGDS PDE1A RND3 SHISA9 CABP2 COL4A2 MGP −9 PDE6H SGK1 NNAT NFIB COL11A1SLIT2 PPP1R17 CCK GABRA1 NR2F2 NEUROD2 −10 NFIB TMEFF2 PDE6H CNTN4IGFBP7 EPHA7 ALCAM GJD2 HS3ST4 COL4A1 MEIS2 −11 PTGDS TPM3 CNGB3 SOX6FAM19A3 CDH9 CACNG4 DYNC1I1 RELN IGFN1 IGF2 −12 KCNE2 SOWAHA KCNE2 RP1GSG1 SOX6 CRABP1 SLC6A9 KCND3 SEPT4 CHODL −13 PTN ARL4C CACNG4 GLRA1JUNB HPGD CAMK4 MAF WLS COX4I2 CDH8 −14 CLU AI593442 OTOR GNB1 NR4A1RND3 B230312C02RIK CACNG4 PRDM8 S1PR3 CALD1 −15 FAM19A3 SLC4A3 PTPRZ1FAM19A3 FOSB WLS 1500016L03RIK SLC17A8 GLRA1 MAF TAC1 −16 OPN1SWTPM3-RS7 KDR VSX2 OTOR SLC17A8 PCDH17 TFAP2B SNCA TFAP2C PRDM13 −17ENPP2 MEIS2 DNER PCDH10 NBL1 COL1A2 FN1 ALCAM FEZF2 ID4 GJC1 −18 NUDT4PTN CLDN5 NFIA ATF3 DYNC1I1 CARTPT OPTC AI593442 2610017I09RIK LGR5 −19SPARC VIM QPN1SW MEST NNAT PCDH10 VIP RGS2 PCDH10 ANXA1 GRIK2 −20 VIMCALB1 VEGFA CST3 NFIB HS3ST4 HS3ST4 NEUROD2 CDH9 ATP1A2 TNNT1 Top andbottom genes PC22 PC23 PC24 PC25 PC26 PC27 PC28 PC29 PC30 PC31 PC32 12610017I09RIK IGF2 CARTPT HBB-BS HPGD PPP1R17 CHN2 PTGDS GJD2 PDLIM3PCDH17 2 NEFH HBA-A1 MAF HBA-A1 IGF2 HBA-A1 RELN GPR22 DYNC1I1 ALDH1A1PMEPA1 3 C1QL2 HBB-BS PPP1R17 2610017I09RIK IGFBP5 HBB-BS DNER CHN2 NPYRBP1 GSG1 4 IGFBP2 VIP GPR22 TAC2 MT2 IGFN1 GRIK1 TTR CCND1 HOPX PPP1R175 THY1 ID4 GNG2 TAC1 CXCL12 EBF1 PCP4L1 GABRA1 FEZF2 ITM2A IGFBP5 6 TBX3CXCL12 NR4A2 C1QL2 2610017I09RIK NETO1 GPR22 CARTPT SLITRK6 GSTA4 HOPX 7GAD1 IGFBP5 IGFBP5 GRIK1 TAC2 ALDH1A1 NNAT SYT7 VSNL1 CHN2 BAI1 8 OLFM3ALDOC GRIK1 CXCL14 LAMP5 VIP DDR1 SCG2 B2M SLC17A8 RBP1 9 KCND3 NR4A2SLC4A4 NXPH1 MT1 PCP4L1 SLITRK6 DNER ARL4C CCND1 UCHL1 10 NFIX CBLN2SNED1 B230312C02RIK NETO1 NPNT PMEPA1 SPOCK3 BHLHE22 DBI LHX4 11 DKK3HS6ST2 CAMK4 LHX2 PTGDS GRIK1 PCDH17 TAC1 2610017I09RIK DAPL1 NFIB 12PMEPA1 IGFBP2 KCND3 GPR22 IGF1 VSX1 SLC6A1 PRDM13 MT1 RDH10 GAS1 13NCKAP5 GRIM1 C1QL1 IGF2 CST3 SLITRK6 SHISA9 PTPRT ELAVL2 PRDX6 DDR1 14ID4 LRRTM1 ID4 LY6C1 LHX4 COL11A1 TAC1 RPRM MT2 GPR22 CALD1 15 SYT7LECT1 GRIA3 ELAVL2 PDE1A CBLN2 SYT7 SHISA9 PTPRF SBSPON VEGFA 16 SOX6CHN2 LGR5 OPTC B2M SEPT4 ZBTB20 MAF NPNT NNAT NR2F2 17 HPGD GABRA2PCP4L1 NFIB ELAVL2 LPL VSTM2B PCDH17 NCKAPS S1PR3 BHLHE22 18 CHODLSLC4A4 DNER NETO1 CHRNA6 COL1A2 PTPRT EBF1 PCDH10 MT2 TBX3 19 SLC17A6SNED1 NF1A TBX3 NNAT A330008L17RIK TNNT1 SERPINE2 ATF3 ANXA1 NR4A1 20SIX3OS1 MLC1 IGFN1 NFIX GSG1 NNAT CCK ID4 DNER RPRM ALDH1A1 −1 TAC2 TAC2HBA-A1 VIP HBB-BS WLS WLS SLC17A8 SLC17A8 GM129 HEXB −2 VIP TAC1 HBB-BSCBLN2 HBA-A1 IGF2 CAR2 PMEPA1 AI593442 ABCA8B SOX6 −3 SYT6 2610017I09RIKPCDH17 WLS WLS PCDH10 PCDH10 LECT1 NXPH1 PTGDS CCK −4 TAC1 CXCL14 CHN2RND3 PCDH10 PCDH17 PPP1R17 HPGD MAF KLF4 HPGD −5 SNCA C1QL2 SLC6A1PPP1R17 VIP LECT1 C1QL2 NEUROD2 LHX2 SHISA9 KCNIP4 −6 FXYD6 CDKN1CELAVL2 CCK CAMK4 CXCL12 RND3 NR2F2 SLC4A4 DIO2 COL11A1 −7 ELAVL2 SNCAPCDH10 RBP1 PRDM8 CAMK4 NXPH1 CBLN2 GRIA3 SNED1 SERPINE2 −8 SERPINE2ALDH1A1 CBLN2 GNB1 NB4A2 ZFHX4 EBF3 CACNG4 NNAT CRIM1 GABRR2 −9 LAMP5SLC17A8 TKT CHN2 PPP1R17 TBX3 RBP1 COL11A1 CXCL14 SLITRK2 WLS −10 IGFBP5SERPINE2 TAC2 UNC13C CCK NFIX B3GALT2 PCDH10 FOS HEXB SLC17A8 −11 GRIA3PMEPA1 HPGD NR4A2 RNF152 GPR22 OLFM3 GABRA2 GABRA2 GAS1 ATF3 −12 NNATMGP MGP HS6ST2 CARTPT PRDM8 HPGD RBFOX1 LAMPS TIMP3 SEPP1 −13 STMN2 WLSMEIS2 RP1 GJD2 TAC1 TTR SLITRK6 ALDOC ENPP2 B2M −14 NR4A2 CALD1 GABRA1HSPA1B CAR2 TACR3 IER5 NFIX CABP2 TTR GRIK1 −15 NECAB1 ELAVL2 SHISA9SHISA9 CCND1 GLRA1 PTPRZ1 CRIM1 PRDM8 HSPA1B A730046J19RIK −16 B2M HPGDCALD1 VWA1 A730046J19RIK EPHA7 CABP2 VIP NR4A2 NRP1 LECT1 −17 IGFN1CCND1 UNC13C PCDH10 ALDH1A1 SLC4A4 B2M VEGFA NEUROD2 PPAP2B SLITRK6 −18CNGB3 S1PR3 RBP1 ALDOC PCDH17 B230312C02RIK CAMK4 IGF2 EGR1 GM26669CACNA2D3 −19 SLC6A9 AI593442 QPCT SEPT4 NPNT B2M C1QL1 DDR1 SCG2 S1PR1MAF −20 CALD1 RELN PTGDS TTR NELL2 2610017I09RIK 2610017I09RIK CCKGM13889 PPP1R17 VIP Top and bottom genes PC33 PC34 PC35 PC36 PC37 PC38PC39 PC40 1 PTPRT ARL4C TTR TPM3-RS7 HEXB TPM3-RS7 CDKN1C SLC17A8 2PCDH10 RPRM GM129 CDKN1C ATF3 TPM3 HSPA1B GM26669 3 TPBG SLC17A8 GM26669TBX3 TTR TAC2 HSPA1A ATF3 4 IGFBP5 NPNT PTGDS RND3 PMEPA1 SHISA9 CXCL12TTR 5 RPRM BHLHE22 KCND3 TPM3 GM26924 RGS2 KLF4 CDKN1C 6 NR2F2 TPM3-RS7VIP ANGEL2 RBP1 NFKBIA TAC2 CALD1 7 LECT1 CAMK4 IGF2 SYT6 B2M NR2F2NR4A2 MT2 8 CDK14 TBX3 TPM3-RS7 PCDH17 MAF ELAVL2 GM26924 TAC2 9 DIO2PTGDS TPM3 TPBG PTGDS IGF1 SHISA9 ADAMTS1 10 TBX3 SLITRK6 CRIM1 IGFN1MT2 MAF HS6ST2 VSTM2B 11 SLITRK6 TPM3 RBP1 NCKAP5 MFKBIZ PPP1R17 NNATUTP14B 12 CDKN1C FILIP1L ANGEL2 GRIK2 KCND3 ID4 RELN CXCL12 13 SHISA9GM26924 ILDR2 NFIX SYT6 HS6ST2 PRDM8 NFKBIZ 14 PTPRF EBF1 SHISA9 NFIBPRDM8 HEXB LRRTM1 CHN2 15 NNAT CHN2 KCNIP4 ALCAM MT1 ILDR2 ID1 DNER 16CALB2 ELAVL2 TRPM3 CAR2 SEPP1 GM26924 WLS ID4 17 SOX6 PRDM13 TAC2 CHN2HOPX NEFH LY6C1 NR2E1 18 GABRA2 RBFOX1 WLS CHBNA6 DDR1 NNAT ALCAM GLRA119 UNC13C GM13889 GRIK2 NEUROD2 SLC4A4 SYT7 CAR2 NXPH1 20 TAC1 LPL FZD5GSG1 KLF6 GLRA1 RGS4 SOWAHA −1 TAC2 AI593442 HEXB PTPRT GM129 TAC1ANDEL2 TPM3-RS7 −2 ELAVL2 SLC4A4 ATF3 TAC2 HSPA1A MT2 SLC17A8 TPM3 −3GRIK2 VIP HSPA1A RBP1 PVRL3 PTGDS LAMB1 HSPAIB −4 NCKAPS MAF HSPA1B TTRCXCL12 HSPA1A SERPINE2 HSPA1A −5 VIP TAC1 CTSH COL11A1 FOS GRIA3 NPYEGR1 −6 NFIX COL11A1 IER5 PMEPA1 NPY HSPA1B TAC1 OLFM3 −7 SCG2 RND3NFKBIA PTPRF SOX6 VIP VIP JUND −8 KCND3 LRRTM1 RGS2 WLS OPTC GM13889NFIB PTGDS −9 PRDM8 IGF1 PCDH17 EPHA7 COL11A1 MT1 PCDH17 FOS −10 CHN2GAD2 SEPP1 SERPINE2 HTRA1 A330069E16RIK IGFBP5 SLIT2 −11 ATP1B3 SYT6PPP1R17 CAMK4 PPP1R15A CXCL12 A330069E16RIK FEZF2 −12 NPY CXCL14 SGK1PDLIM3 PPP1R17 KLF4 CARTPT DDR1 −13 MAF TPBG GPR22 HOPX NBL1 PCDH10 HEXBSIX3OS1 −14 TFAP2B CHRNA6 LHX2 BAI1 DUSP6 CDKN1C GPR22 HOPX −15 NEUROD2SERPINE2 SERPINE2 LRRTM1 A330069E16RIK TKT CNGB3 TAC1 −16 CRABP1 CBLN2DDR1 CARTPT CROT TPBG VWA1 CBLN2 −17 ALDOC PDLIM3 SLC17A8 IGFBP2 HSPA1BKCND3 GM129 PDLIM3 −18 NPNT SCG2 SAT1 NPY PTN CHRNA6 CABP2 RPRM −19FXYD6 HS6ST2 PON2 A730046J19RIK PTPRT NHLH2 FZD5 SLC6A9 −20 DKK3 PTPRFB2M HSPA1B GPX8 BHLHE22 GRIA3 PDE1A

TABLE 6 Genes differentially expressed in each of the 39 retinal cellclusters. myAUC myDiff power cluster # cluster no. 1 DE = 190 CALB10.966 3.615047 0.466 1 SLC4A3 0.963 3.448571 0.463 1 TPM3 0.965 3.1515210.465 1 SEPT4 0.964 2.939258 0.464 1 VIM 0.944 2.937992 0.444 1 SEPT70.968 2.808893 0.468 1 1500016L03RIK 0.896 2.777389 0.396 1 LHX1 0.8622.524691 0.362 1 ATP1B1 0.913 2.520540 0.413 1 BAI1 0.855 2.451809 0.3551 CD47 0.904 2.425913 0.404 1 TPM3-RS7 0.850 2.340003 0.350 1 SNHG110.906 2.329016 0.406 1 PCSK1N 0.910 2.295309 0.410 1 C1QL1 0.8632.257023 0.363 1 PPP1R1A 0.872 2.200677 0.372 1 NEBL 0.840 2.1879730.340 1 MAGED1 0.901 2.143543 0.401 1 GNAS 0.936 2.121058 0.436 1 PCBD10.837 2.100263 0.337 1 TMEFF2 0.837 2.087888 0.337 1 SMARCA4 0.9072.073006 0.407 1 LRRC4 0.833 2.057230 0.333 1 UTRN 0.803 1.995075 0.3031 ADRA2A 0.813 1.993091 0.313 1 TFAP2B 0.899 1.986766 0.399 1 MYO6 0.8601.972649 0.360 1 NDRG4 0.882 1.970533 0.382 1 GNG2 0.825 1.959108 0.3251 TMEM132A 0.816 1.954705 0.316 1 GM16551 0.799 1.945718 0.299 1 ONECUT20.807 1.931103 0.307 1 NDRG1 0.906 1.920706 0.406 1 A330050F15RIK 0.8041.915932 0.304 1 TKT 0.855 1.910653 0.355 1 COL27A1 0.726 1.883251 0.2261 SGK1 0.821 1.876982 0.321 1 FAM126A 0.802 1.858034 0.302 1 WNK4 0.7841.841538 0.284 1 TAGLN3 0.815 1.782407 0.315 1 SLC12A2 0.803 1.7683140.303 1 SLC4A5 0.781 1.760906 0.281 1 LSAMP 0.829 1.738595 0.329 1 SYT20.779 1.713377 0.279 1 LY6E 0.747 1.701416 0.247 1 STMN2 0.827 1.6971690.327 1 LMO1 0.769 1.657498 0.269 1 SEPT8 0.784 1.654456 0.284 1 PROX10.846 1.646287 0.346 1 CHGB 0.841 1.628412 0.341 1 NPY 0.737 1.6271930.237 1 GALNT18 0.765 1.620340 0.265 1 ZEB2 0.793 1.616501 0.293 1SOWAHA 0.752 1.605413 0.252 1 LIMA1 0.773 1.599290 0.273 1 THRSP 0.7581.592738 0.258 1 MEGF11 0.765 1.587717 0.265 1 UCHL1 0.809 1.5857990.309 1 F2R 0.742 1.585087 0.242 1 RCN2 0.798 1.581440 0.298 1 VWC20.763 1.571960 0.263 1 PCSK6 0.735 1.571878 0.235 1 ITGB5 0.745 1.5575120.245 1 APP 0.822 1.550700 0.322 1 TUBB2A 0.817 1.540466 0.317 1BC030476 0.750 1.535140 0.250 1 CDC42EP4 0.754 1.512842 0.254 1 PTPRO0.748 1.502980 0.248 1 RGS3 0.746 1.501006 0.246 1 2410066E13RIK 0.7681.487613 0.268 1 WFDC10 0.718 1.485101 0.218 1 ANK2 0.855 1.477172 0.3551 CTTNBP2 0.741 1.474312 0.241 1 FAM124A 0.721 1.474108 0.221 1 TNR0.729 1.463381 0.229 1 RBFOX2 0.768 1.456189 0.268 1 SPARCL1 0.7671.446874 0.267 1 THSD7A 0.783 1.441073 0.283 1 PACSIN1 0.799 1.4403950.299 1 VAT1L 0.751 1.429302 0.251 1 SYT11 0.786 1.425350 0.286 1 AKAP120.739 1.424278 0.239 1 ABHD10 0.763 1.411246 0.263 1 PTPRT 0.7291.406432 0.229 1 RCAN2 0.754 1.405642 0.254 1 KIF3A 0.793 1.398151 0.2931 LRP11 0.758 1.397326 0.258 1 RTN1 0.801 1.393281 0.301 1 FKBP3 0.8071.383785 0.307 1 NEFL 0.814 1.374162 0.314 1 CD59A 0.753 1.372191 0.2531 CDH4 0.748 1.371678 0.248 1 TMOD1 0.746 1.367990 0.246 1 FAIM2 0.7511.367737 0.251 1 CTNNA2 0.739 1.362929 0.239 1 SEPT6 0.737 1.3575960.237 1 MAB21L2 0.751 1.352143 0.251 1 MSI2 0.844 1.351412 0.344 1ONECUT1 0.723 1.348846 0.223 1 ANGPT2 0.716 1.342637 0.216 1 THSD7B0.709 1.318613 0.209 1 SNAP25 0.905 1.316286 0.405 1 NEFM 0.766 1.3111340.266 1 SCD2 0.753 1.296970 0.253 1 FAM84B 0.734 1.296355 0.234 1 MGARP0.888 1.277813 0.388 1 APPL2 0.758 1.261116 0.258 1 DNER 0.752 1.2560050.252 1 PFKFB3 0.706 1.250256 0.206 1 MT1 0.729 1.246724 0.229 1 LMO40.742 1.245222 0.242 1 ZFP804A 0.746 1.241753 0.246 1 RABEP1 0.7711.228045 0.271 1 OSBPL1A 0.729 1.227105 0.229 1 YWHAG 0.763 1.2251120.263 1 PDE3A 0.702 1.219989 0.202 1 CACNG3 0.717 1.219146 0.217 1 REEP50.751 1.204753 0.251 1 KLF13 0.706 1.196781 0.206 1 TMX4 0.753 1.1867790.253 1 SNCG 0.712 1.184574 0.212 1 SNRPN 0.732 1.180677 0.232 1 SLC24A20.705 1.172493 0.205 1 GNAI1 0.726 1.153326 0.226 1 MLLT11 0.7331.153193 0.233 1 DST 0.742 1.150327 0.242 1 ADARB1 0.742 1.147777 0.2421 ANKRD29 0.706 1.145796 0.206 1 ST8SIA3 0.703 1.129373 0.203 1 PLCB40.765 1.116768 0.265 1 BEX2 0.762 1.114780 0.262 1 FAM115A 0.7461.114026 0.246 1 PLEKHA1 0.751 1.113187 0.251 1 MPC1 0.706 1.1096700.206 1 MOCS2 0.739 1.107821 0.239 1 COX5A 0.776 1.104444 0.276 1 TUBA1A0.774 1.100378 0.274 1 PLCH1 0.705 1.097744 0.205 1 PIK3R3 0.7111.092873 0.211 1 TSPAN3 0.771 1.087383 0.271 1 EMC9 0.703 1.086119 0.2031 UHRF1BP1L 0.710 1.081116 0.210 1 NAV1 0.713 1.074276 0.213 1 INA 0.7241.066690 0.224 1 HAUS8 0.708 1.065310 0.208 1 HSP90AB1 0.800 1.0596810.300 1 NDN 0.733 1.058386 0.233 1 NEFH 0.707 1.052242 0.207 1 GATSL20.702 1.046289 0.202 1 TPM1 0.728 1.044557 0.228 1 STMN3 0.743 1.0424090.243 1 ZWINT 0.717 1.028737 0.217 1 SPOCK3 0.704 1.026265 0.204 1ELAVL3 0.730 1.019721 0.230 1 ATP6V1A 0.761 1.013906 0.261 1 LDHA 0.298−1.429546 0.202 1 H3F3B 0.226 −1.724698 0.274 1 EPB4.1 0.297 −1.8903300.203 1 A930011O12RIK 0.289 −1.908058 0.211 1 TMA7 0.292 −1.922734 0.2081 CRX 0.295 −1.940202 0.205 1 HMGN1 0.173 −2.030775 0.327 1 MPP4 0.297−2.122800 0.203 1 CNGB1 0.289 −2.144480 0.211 1 FAM57B 0.269 −2.1486140.231 1 GUCA1B 0.298 −2.192529 0.202 1 AIPL1 0.269 −2.202228 0.231 1PDE6A 0.284 −2.233229 0.216 1 RDH12 0.291 −2.272536 0.209 1 GNB1 0.187−2.284490 0.313 1 NEUROD1 0.238 −2.422956 0.262 1 NRL 0.224 −2.4244090.276 1 UNC119 0.193 −2.478130 0.307 1 NR2E3 0.217 −2.484357 0.283 1 RS10.222 −2.534411 0.278 1 SLC24A1 0.230 −2.558786 0.270 1 PRPH2 0.154−2.572327 0.346 1 ROM1 0.184 −2.594330 0.316 1 RP1 0.190 −2.660436 0.3101 PDE6B 0.190 −2.707960 0.310 1 TULP1 0.163 −2.748272 0.337 1 CNGA10.215 −2.752815 0.285 1 RCVRN 0.175 −2.769719 0.325 1 PDE6G 0.160−2.791625 0.340 1 PDC 0.133 −2.805456 0.367 1 GNGT1 0.123 −2.8211790.377 1 RPGRIP1 0.195 −2.867157 0.305 1 GNAT1 0.158 −2.923872 0.342 1RHO 0.121 −2.940345 0.379 1 SAG 0.118 −2.967888 0.382 1 cluster no. 2 DE= 174 NEFL 0.984 3.829399 0.484 2 NEFM 0.953 3.464532 0.453 2 SNCG 0.9383.269859 0.438 2 CALB2 0.884 3.081448 0.384 2 STMN2 0.944 2.861225 0.4442 THY1 0.900 2.782679 0.400 2 ATP1B1 0.916 2.633335 0.416 2 SLC17A60.879 2.610603 0.379 2 NRN1 0.868 2.509114 0.368 2 UCHL1 0.909 2.4119260.409 2 GAP43 0.867 2.314068 0.367 2 STMN3 0.906 2.200448 0.406 2 CDK140.855 2.189091 0.355 2 YWHAH 0.854 2.103748 0.354 2 RGS4 0.775 2.0524110.275 2 NELL2 0.801 2.005519 0.301 2 SNHG11 0.847 1.998298 0.347 2 RTN10.872 1.992219 0.372 2 FXYD7 0.815 1.921975 0.315 2 INA 0.857 1.8646470.357 2 TPPP3 0.789 1.858532 0.289 2 TUBB2A 0.851 1.844621 0.351 2 RBPMS0.796 1.835589 0.296 2 MEG3 0.835 1.831667 0.335 2 SCN2A1 0.798 1.8252590.298 2 TUBB3 0.814 1.819493 0.314 2 VSNL1 0.793 1.812314 0.293 2 APP0.848 1.800057 0.348 2 MFSD6 0.791 1.774345 0.291 2 OLFM1 0.832 1.7671420.332 2 CEND1 0.806 1.753636 0.306 2 KIF5A 0.806 1.715671 0.306 2 ZWINT0.822 1.713431 0.322 2 BASP1 0.839 1.707778 0.339 2 CHRNA6 0.7511.703049 0.251 2 NAP1L5 0.826 1.688741 0.326 2 SCN1A 0.761 1.6754140.261 2 SPARCL1 0.806 1.650738 0.306 2 RAB6B 0.826 1.648695 0.326 2 SNCA0.746 1.628302 0.246 2 DNER 0.806 1.625146 0.306 2 MYT1L 0.782 1.6021850.282 2 TAGLN3 0.789 1.596353 0.289 2 NSG2 0.791 1.591428 0.291 2 NDRG40.818 1.579659 0.318 2 KCNIP4 0.724 1.575295 0.224 2 MAP1A 0.7611.564301 0.261 2 FGF12 0.759 1.554984 0.259 2 CPLX2 0.757 1.547165 0.2572 LSAMP 0.764 1.532664 0.264 2 NSG1 0.773 1.531646 0.273 2 GNG3 0.7981.526804 0.298 2 TTC3 0.863 1.526759 0.363 2 SNRPN 0.786 1.524628 0.2862 MGST3 0.763 1.521974 0.263 2 POU4F1 0.708 1.493041 0.208 2 RBFOX10.756 1.490707 0.256 2 2900011O08RIK 0.797 1.489750 0.297 2 S100A100.739 1.487422 0.239 2 CALM2 0.848 1.470176 0.348 2 CPLX1 0.711 1.4588790.211 2 CAMK2N1 0.791 1.455445 0.291 2 GABBR2 0.734 1.435871 0.234 2RBPMS2 0.735 1.422357 0.235 2 ELAVL2 0.716 1.416182 0.216 2 REEP5 0.7671.411279 0.267 2 ACOT7 0.763 1.408963 0.263 2 LYNX1 0.732 1.398066 0.2322 CHRNB3 0.724 1.396429 0.224 2 RAB6A 0.802 1.365048 0.302 2 SYT11 0.7891.361853 0.289 2 RPH3A 0.769 1.361064 0.269 2 MGLL 0.731 1.351262 0.2312 CAPNS1 0.766 1.336082 0.266 2 ELAVL4 0.739 1.327648 0.239 2 MLLT110.754 1.324574 0.254 2 APBB2 0.733 1.324301 0.233 2 HPCA 0.735 1.3124420.235 2 PPP2R2C 0.729 1.312231 0.229 2 MYO1B 0.703 1.310809 0.203 2PCDHA2 0.752 1.310031 0.252 2 SULT4A1 0.720 1.305228 0.220 2 ROBO2 0.7351.276553 0.235 2 ATL1 0.728 1.276524 0.228 2 YWHAB 0.828 1.272542 0.3282 BEND6 0.719 1.270603 0.219 2 AHNAK2 0.713 1.266931 0.213 2 TUBA1A0.825 1.258349 0.325 2 RESP18 0.702 1.244231 0.202 2 NRXN1 0.7191.242874 0.219 2 ATP2B2 0.719 1.240608 0.219 2 EPHA5 0.723 1.2310670.223 2 SPOCK2 0.735 1.228244 0.235 2 TMEM130 0.726 1.225743 0.226 2YWHAG 0.751 1.224966 0.251 2 SRGAP1 0.707 1.220082 0.207 2 STMN4 0.7221.214691 0.222 2 GNAS 0.823 1.206586 0.323 2 EBF1 0.717 1.202313 0.217 2KIF5C 0.748 1.199040 0.248 2 TPM1 0.735 1.195887 0.235 2 TTLL7 0.7071.194259 0.207 2 HSP90AB1 0.844 1.192653 0.344 2 ENO2 0.784 1.1907770.284 2 INPP5F 0.710 1.175178 0.210 2 L1CAM 0.714 1.174820 0.214 2SERINC1 0.776 1.172132 0.276 2 KIFAP3 0.781 1.169721 0.281 2 TMSB100.748 1.167262 0.248 2 ATPIF1 0.773 1.160103 0.273 2 MAPT 0.751 1.1535920.251 2 EMB 0.704 1.153408 0.204 2 SYN2 0.713 1.152558 0.213 2 CALM30.757 1.147375 0.257 2 SCG2 0.767 1.144454 0.267 2 RAB3C 0.735 1.1438690.235 2 TMOD2 0.733 1.143826 0.233 2 PCP4 0.743 1.137348 0.243 2 LDHB0.729 1.136283 0.229 2 OGFRL1 0.728 1.132671 0.228 2 PLS3 0.701 1.1292420.201 2 OSBPL1A 0.713 1.127818 0.213 2 SYT4 0.736 1.109372 0.236 2 CD470.749 1.108135 0.249 2 CNTN1 0.716 1.100946 0.216 2 SPOCK3 0.7131.096385 0.213 2 KLC1 0.761 1.081218 0.261 2 DPYSL2 0.722 1.070807 0.2222 CBX6 0.706 1.069450 0.206 2 GNAO1 0.801 1.066166 0.301 2 RBFOX3 0.7061.062023 0.206 2 SEPT3 0.710 1.061409 0.210 2 RTN3 0.764 1.054404 0.2642 TXN1 0.741 1.045930 0.241 2 CYGB 0.712 1.041602 0.212 2 DSTN 0.7361.028947 0.236 2 NEFH 0.701 1.028807 0.201 2 EPB4.1L3 0.735 1.0245610.235 2 NDN 0.729 1.022810 0.229 2 YWHAQ 0.735 1.021231 0.235 2 ATP6V1G20.713 1.019868 0.213 2 CYB5R3 0.702 1.016407 0.202 2 GPRASP1 0.7421.013893 0.242 2 RIT2 0.711 1.012204 0.211 2 PDCD4 0.741 1.004699 0.2412 H3F3B 0.271 −1.176930 0.229 2 DDX5 0.276 −1.193109 0.224 2 GNB1 0.239−1.628273 0.261 2 TMA7 0.290 −1.756221 0.210 2 PDE6A 0.298 −1.9165180.202 2 RDH12 0.299 −1.978256 0.201 2 NEUROD1 0.265 −1.982771 0.235 2AIPL1 0.277 −2.036910 0.223 2 NRL 0.241 −2.048768 0.259 2 CRX 0.293−2.064793 0.207 2 CNGA1 0.239 −2.128658 0.261 2 RS1 0.239 −2.1326050.261 2 UNC119 0.212 −2.193079 0.288 2 HMGN1 0.156 −2.204076 0.344 2ROM1 0.206 −2.223073 0.294 2 SLC24A1 0.243 −2.273294 0.257 2 NR2E3 0.229−2.289315 0.271 2 TULP1 0.174 −2.369311 0.326 2 PDE6B 0.202 −2.3914140.298 2 PDE6G 0.180 −2.394168 0.320 2 RP1 0.203 −2.416303 0.297 2 PRPH20.164 −2.440696 0.336 2 RCVRN 0.183 −2.450023 0.317 2 GNAT1 0.175−2.524310 0.325 2 RHO 0.130 −2.595284 0.370 2 SAG 0.129 −2.599480 0.3712 GNGT1 0.129 −2.621825 0.371 2 RPGRIP1 0.204 −2.684191 0.296 2 PDC0.139 −2.696102 0.361 2 cluster no. 3 DE = 162 RIMS1 0.992 4.0822150.492 3 CALB2 0.959 3.407422 0.459 3 SCG2 0.951 2.785881 0.451 3 NPY0.904 2.685796 0.404 3 SPOCK3 0.945 2.678047 0.445 3 SNHG11 0.9422.664892 0.442 3 SLC5A7 0.889 2.523739 0.389 3 GAD1 0.893 2.305332 0.3933 PCP4 0.927 2.304931 0.427 3 ATP1B1 0.915 2.244273 0.415 3 GNG7 0.8722.199902 0.372 3 SPARCL1 0.877 2.152659 0.377 3 CHAT 0.839 2.1177640.339 3 IGFBP7 0.874 2.106632 0.374 3 KCNC1 0.862 2.034054 0.362 3CXCL14 0.836 2.027676 0.336 3 RBFOX1 0.842 2.010200 0.342 3 NHLH2 0.8571.965244 0.357 3 PCP4L1 0.858 1.946188 0.358 3 HECW1 0.840 1.9327960.340 3 RGS7BP 0.817 1.924553 0.317 3 MEGF11 0.822 1.915714 0.322 3LSAMP 0.846 1.876113 0.346 3 GABRD 0.818 1.867550 0.318 3 CACNA2D1 0.8171.822163 0.317 3 ID4 0.811 1.814870 0.311 3 CMTM8 0.807 1.803043 0.307 3KCNAB1 0.797 1.796360 0.297 3 PPFIBP1 0.812 1.772586 0.312 3 ZMAT4 0.8091.764427 0.309 3 TGFB3 0.799 1.762589 0.299 3 RPH3A 0.864 1.751654 0.3643 NNAT 0.826 1.742048 0.326 3 CALB1 0.822 1.723125 0.322 3 CACNG2 0.8011.702459 0.301 3 CALM1 0.934 1.694273 0.434 3 PCDH10 0.781 1.6881720.281 3 PAPPA2 0.743 1.682248 0.243 3 SOX2OT 0.798 1.681475 0.298 3 SCG30.850 1.653641 0.350 3 DLGAP1 0.805 1.626709 0.305 3 CHN1 0.835 1.6175820.335 3 GPR123 0.778 1.617023 0.278 3 FAM184B 0.787 1.601364 0.287 3SLC32A1 0.796 1.599822 0.296 3 COL25A1 0.764 1.584211 0.264 3 PPM1L0.775 1.568651 0.275 3 CHGB 0.881 1.563185 0.381 3 MEG3 0.866 1.5631140.366 3 GABRA2 0.758 1.561233 0.258 3 CNTNAP2 0.811 1.558861 0.311 3LIN7A 0.837 1.506146 0.337 3 CAMK2N1 0.830 1.503683 0.330 3A830010M20R1K 0.761 1.495505 0.261 3 APBA1 0.756 1.494915 0.256 3 CPLX20.795 1.493169 0.295 3 MAGI3 0.762 1.479676 0.262 3 CTTNBP2 0.7801.474337 0.280 3 SLC6A1 0.797 1.471722 0.297 3 TFAP2B 0.838 1.4583290.338 3 GABRA4 0.731 1.443690 0.231 3 ISL1 0.866 1.442516 0.366 3 FAM49B0.785 1.430077 0.285 3 CAMK2A 0.736 1.425387 0.236 3 CDK14 0.7731.414271 0.273 3 GSTO1 0.715 1.408011 0.215 3 GRIA3 0.746 1.402325 0.2463 TENM2 0.740 1.390000 0.240 3 CAPZA2 0.805 1.363952 0.305 3 TAGLN30.781 1.361440 0.281 3 SYT11 0.787 1.343219 0.287 3 GALNT15 0.7181.338314 0.218 3 MAPK10 0.747 1.333658 0.247 3 SOX2 0.748 1.328242 0.2483 GRIA2 0.810 1.314674 0.310 3 SNRPN 0.765 1.302095 0.265 3 STXBP6 0.7151.300343 0.215 3 PSD3 0.724 1.295147 0.224 3 BASP1 0.786 1.289016 0.2863 ARL4C 0.730 1.279132 0.230 3 SYNPR 0.776 1.278017 0.276 3 HLF 0.7821.276773 0.282 3 NAP1L5 0.796 1.275991 0.296 3 APP 0.736 1.275816 0.2363 NREP 0.818 1.271487 0.318 3 PTPRD 0.801 1.264783 0.301 3 NRCAM 0.7421.263960 0.242 3 CD47 0.788 1.255114 0.288 3 PODXL2 0.767 1.235972 0.2673 STMN3 0.779 1.235054 0.279 3 NEFH 0.713 1.230658 0.213 3 DAPK1 0.7261.224896 0.226 3 ELAVL3 0.770 1.220472 0.270 3 VSTM2A 0.709 1.2203170.209 3 REEP5 0.747 1.212653 0.247 3 CYFIP2 0.737 1.198555 0.237 3AMIGO2 0.719 1.193345 0.219 3 GNG3 0.783 1.192467 0.283 3 CHD3 0.7581.190095 0.258 3 DTNB 0.717 1.187726 0.217 3 NPTN 0.778 1.186421 0.278 3DIRAS2 0.721 1.182766 0.221 3 PGM2L1 0.750 1.178870 0.250 3 KIF5C 0.7601.178481 0.260 3 SYT1 0.855 1.177984 0.355 3 LDHB 0.778 1.172023 0.278 3ELMOD1 0.748 1.164081 0.248 3 PLCH1 0.704 1.162078 0.204 3 EDIL3 0.7251.160835 0.225 3 NRXN2 0.766 1.157403 0.266 3 FAM115A 0.738 1.1552080.238 3 MED12L 0.710 1.151691 0.210 3 MXRA7 0.776 1.145751 0.276 3 DNM30.796 1.143089 0.296 3 VSTM2L 0.703 1.141293 0.203 3 1700025G04R1K 0.7231.129913 0.223 3 ATP2B2 0.721 1.129631 0.221 3 SNCB 0.786 1.128583 0.2863 TTC3 0.820 1.121625 0.320 3 SV2A 0.778 1.119631 0.278 3 MGLL 0.7311.117164 0.231 3 ESPN 0.725 1.107524 0.225 3 FEZ1 0.713 1.105736 0.213 3CELF4 0.802 1.102736 0.302 3 TMEM191C 0.709 1.102454 0.209 3 PRAF2 0.7191.093227 0.219 3 CYGB 0.729 1.086962 0.229 3 PCDHA2 0.724 1.084084 0.2243 GPM6A 0.774 1.076995 0.274 3 SEPT11 0.701 1.075883 0.201 3 ZCCHC180.727 1.075250 0.227 3 6430548M08RIK 0.736 1.071386 0.236 3 ITM2C 0.7541.051279 0.254 3 ATP6V1E1 0.784 1.048681 0.284 3 SLC4A10 0.714 1.0480670.214 3 GABRB3 0.707 1.045363 0.207 3 HPCAL1 0.723 1.028678 0.223 3CACNA2D2 0.710 1.018877 0.210 3 YWHAH 0.728 1.009599 0.228 3 CST3 0.282−1.475405 0.218 3 GNB1 0.240 −1.654043 0.260 3 HMGN1 0.189 −1.8276490.311 3 AIPL1 0.290 −1.857153 0.210 3 RCVRN 0.207 −2.042189 0.293 3UNC119 0.221 −2.055898 0.279 3 NRL 0.242 −2.067154 0.258 3 CNGA1 0.240−2.096207 0.260 3 ROM1 0.209 −2.116826 0.291 3 NR2E3 0.240 −2.1362880.260 3 PDC 0.166 −2.152007 0.334 3 PDE6G 0.192 −2.152778 0.308 3 PDE6B0.213 −2.158794 0.287 3 SLC24A1 0.253 −2.169851 0.247 3 RP1 0.215−2.179412 0.285 3 TULP1 0.186 −2.181446 0.314 3 RPGRIP1 0.226 −2.2036670.274 3 RS1 0.237 −2.206460 0.263 3 PRPH2 0.177 −2.226499 0.323 3 GNGT10.154 −2.289551 0.346 3 GNAT1 0.187 −2.336430 0.313 3 SAG 0.143−2.366434 0.357 3 RHO 0.148 −2.382665 0.352 3 cluster no. 4 DE = 84 TAC10.957 3.797157 0.457 4 CALB2 0.901 2.593063 0.401 4 SNHG11 0.9242.325381 0.424 4 IGFBP7 0.837 2.280199 0.337 4 PAX6 0.913 2.258708 0.4134 NHLH2 0.869 2.201437 0.369 4 GRIA2 0.915 2.170104 0.415 4 AI5934420.810 2.066669 0.310 4 PCP4 0.892 2.063350 0.392 4 SPOCK3 0.845 2.0171150.345 4 COL25A1 0.778 1.916207 0.278 4 KCTD12 0.742 1.898538 0.242 4CXCL14 0.765 1.846094 0.265 4 OGFRL1 0.824 1.840851 0.324 4 GBX2 0.7261.819879 0.226 4 LHX9 0.757 1.816715 0.257 4 KCNIP4 0.751 1.748102 0.2514 TKT 0.815 1.737069 0.315 4 PCDH8 0.704 1.720415 0.204 4 CELF4 0.8961.718605 0.396 4 STMN2 0.794 1.687253 0.294 4 MEG3 0.889 1.662832 0.3894 DNER 0.808 1.653824 0.308 4 ZFHX3 0.765 1.644741 0.265 4 A830036E02RIK0.710 1.606762 0.210 4 SIX6 0.755 1.580762 0.255 4 NDRG4 0.824 1.5632050.324 4 HLF 0.782 1.551737 0.282 4 GRIN2B 0.702 1.522238 0.202 4 SNCA0.734 1.483602 0.234 4 SERPINI1 0.734 1.415131 0.234 4 LY6H 0.7011.377466 0.201 4 GRIA4 0.724 1.373989 0.224 4 SPARCL1 0.724 1.3584430.224 4 NSG2 0.727 1.353166 0.227 4 CDK14 0.720 1.340365 0.220 4 SCN3A0.708 1.309240 0.208 4 NRXN2 0.734 1.297254 0.234 4 NAV1 0.714 1.2899890.214 4 ATP1B1 0.800 1.284113 0.300 4 STXBP5 0.719 1.259255 0.219 4ELAVL3 0.761 1.253246 0.261 4 NUDT4 0.751 1.236266 0.251 4 CALM1 0.8811.220586 0.381 4 PNMAL2 0.728 1.206131 0.228 4 APP 0.774 1.200908 0.2744 TTC3 0.829 1.190737 0.329 4 BASP1 0.744 1.183024 0.244 4 RPH3A 0.7171.156227 0.217 4 CYGB 0.704 1.143763 0.204 4 GPM6A 0.730 1.143690 0.2304 AGAP1 0.713 1.142972 0.213 4 AUTS2 0.704 1.127089 0.204 4 RTN1 0.7671.123584 0.267 4 SLC6A1 0.704 1.115752 0.204 4 SLC22A17 0.712 1.1120670.212 4 SOX4 0.725 1.096108 0.225 4 ANK3 0.747 1.082388 0.247 4 NAP1L50.711 1.054049 0.211 4 CALM2 0.785 1.011094 0.285 4 MARCKSL1 0.7111.007890 0.211 4 LDHA 0.288 −1.329895 0.212 4 HMGN1 0.234 −1.3628950.266 4 UNC119 0.256 −1.364415 0.244 4 NEUROD1 0.269 −1.652305 0.231 4GNB1 0.221 −1.671553 0.279 4 SLC24A1 0.275 −1.699003 0.225 4 RS1 0.266−1.730768 0.234 4 RPGRIP1 0.250 −1.738476 0.250 4 TULP1 0.212 −1.7627160.288 4 NR2E3 0.250 −1.799965 0.250 4 GNAT1 0.216 −1.817149 0.284 4CNGA1 0.253 −1.822516 0.247 4 NRL 0.252 −1.843815 0.248 4 RCVRN 0.213−1.877735 0.287 4 PRPH2 0.190 −1.894117 0.310 4 RHO 0.169 −1.9174250.331 4 ROM1 0.213 −1.930023 0.287 4 RP1 0.231 −1.971244 0.269 4 PDE6G0.206 −2.001563 0.294 4 SAG 0.159 −2.004070 0.341 4 PDE6B 0.223−2.036922 0.277 4 GNGT1 0.164 −2.084646 0.336 4 PDC 0.163 −2.1709460.337 4 cluster no. 5 DE = 159 CALB2 0.823 3.123037 0.323 5 TAC1 0.8332.626378 0.333 5 TPBG 0.876 2.533358 0.376 5 C1QL1 0.924 2.527843 0.4245 CXCL14 0.901 2.230271 0.401 5 SYNPR 0.925 2.131719 0.425 5 STMN2 0.8862.086199 0.386 5 PCDH10 0.797 2.043265 0.297 5 SNHG11 0.922 2.0358220.422 5 NRXN3 0.923 2.007402 0.423 5 CHGB 0.916 2.006283 0.416 5 DLGAP10.862 1.951491 0.362 5 GAD1 0.895 1.927132 0.395 5 SLC6A1 0.882 1.9172320.382 5 ATP1B1 0.889 1.878433 0.389 5 GRIA3 0.852 1.861206 0.352 5AI593442 0.831 1.830170 0.331 5 PAX6 0.867 1.815993 0.367 5 MEIS2 0.8881.783257 0.388 5 DTNBP1 0.850 1.781289 0.350 5 MEG3 0.905 1.740870 0.4055 SLC32A1 0.859 1.720626 0.359 5 CD47 0.872 1.714293 0.372 5 LSAMP 0.8471.699605 0.347 5 2900011O08RIK 0.840 1.682621 0.340 5 RPH3A 0.8651.676398 0.365 5 NRXN2 0.862 1.671095 0.362 5 ZFHX3 0.794 1.649873 0.2945 CDK5R1 0.856 1.647661 0.356 5 GAD2 0.798 1.638829 0.298 5 FILIP1L0.769 1.637232 0.269 5 B2M 0.800 1.608359 0.300 5 P2RY1 0.777 1.5856370.277 5 NSG2 0.825 1.585339 0.325 5 OGFRL1 0.850 1.573178 0.350 5 STMN10.823 1.572466 0.323 5 C1QL2 0.769 1.565457 0.269 5 ZEB2 0.831 1.5445230.331 5 NHLH2 0.808 1.538909 0.308 5 SYT7 0.808 1.527501 0.308 5 RGS80.796 1.505359 0.296 5 ELAVL3 0.838 1.485639 0.338 5 UACA 0.774 1.4757380.274 5 SYT6 0.747 1.459682 0.247 5 CPLX2 0.827 1.458139 0.327 5 FRMD50.787 1.433194 0.287 5 FAM19A5 0.762 1.430612 0.262 5 BHLHE22 0.7641.426500 0.264 5 TUBB2A 0.822 1.419453 0.322 5 VSNL1 0.804 1.4146480.304 5 STXBP6 0.747 1.412450 0.247 5 PCDH8 0.731 1.408067 0.231 5 TKT0.843 1.399775 0.343 5 BASP1 0.828 1.397467 0.328 5 EPB4.1L4A 0.7631.393019 0.263 5 A030009H04RIK 0.803 1.387965 0.303 5 GPM6A 0.8411.376807 0.341 5 NAP1L5 0.808 1.375097 0.308 5 PCDH17 0.799 1.3693590.299 5 GABBR2 0.754 1.368149 0.254 5 SYT11 0.845 1.347546 0.345 5 LRRN30.721 1.338672 0.221 5 CALB1 0.776 1.334921 0.276 5 SV2A 0.850 1.3326360.350 5 SCN3A 0.760 1.325687 0.260 5 RYR2 0.782 1.321029 0.282 5 HUNK0.729 1.315880 0.229 5 BAI3 0.725 1.314119 0.225 5 PCSK2 0.737 1.3113120.237 5 ADCY2 0.739 1.311003 0.239 5 GNG3 0.799 1.308365 0.299 5 TFAP2A0.759 1.308229 0.259 5 ZMAT4 0.754 1.305568 0.254 5 FLRT3 0.763 1.3041170.263 5 GABRA3 0.746 1.300341 0.246 5 DPP6 0.780 1.298661 0.280 5RASGRF1 0.745 1.298565 0.245 5 SPOCK3 0.705 1.294629 0.205 5 CELF4 0.8421.286985 0.342 5 SPARCL1 0.778 1.281146 0.278 5 ELAVL4 0.751 1.2748540.251 5 GRIA4 0.784 1.270207 0.284 5 PKIA 0.775 1.269100 0.275 5 ATRNL10.720 1.259867 0.220 5 UCHL1 0.773 1.241952 0.273 5 CRHR2 0.708 1.2274190.208 5 GRIA2 0.817 1.223394 0.317 5 CACNG3 0.750 1.222476 0.250 5 CDH40.729 1.217037 0.229 5 NDRG4 0.774 1.214021 0.274 5 8430419L09RIK 0.7181.208866 0.218 5 STMN3 0.783 1.205826 0.283 5 NRXN1 0.744 1.199941 0.2445 DIO2 0.722 1.194141 0.222 5 ANK3 0.796 1.193807 0.296 5 DPYSL4 0.7771.187574 0.277 5 STMN4 0.747 1.182336 0.247 5 ROBO2 0.705 1.181819 0.2055 CLMP 0.760 1.181079 0.260 5 UTRN 0.733 1.177432 0.233 5 MLLT11 0.7561.174966 0.256 5 RELN 0.707 1.172184 0.207 5 STK32B 0.712 1.171383 0.2125 ATP1A1 0.773 1.171164 0.273 5 TMX4 0.773 1.170468 0.273 5 GAP43 0.7391.169587 0.239 5 PLCB1 0.709 1.165435 0.209 5 SCN2A1 0.727 1.1618470.227 5 CDK14 0.755 1.157752 0.255 5 UBASH3B 0.731 1.143693 0.231 5MYT1L 0.730 1.141047 0.230 5 6330403K07RIK 0.723 1.140026 0.223 5 TTC30.833 1.133517 0.333 5 FGF14 0.708 1.123639 0.208 5 NRCAM 0.715 1.1219370.215 5 LPHN3 0.733 1.121325 0.233 5 NRSN1 0.758 1.116765 0.258 5 BRINP10.731 1.116028 0.231 5 DCLK1 0.745 1.111968 0.245 5 SUSD4 0.709 1.1110550.209 5 4833424O15RIK 0.722 1.108714 0.222 5 CHGA 0.776 1.098459 0.276 5PBX1 0.777 1.097487 0.277 5 KIF5C 0.747 1.090766 0.247 5 PCP4 0.8291.082855 0.329 5 SNCA 0.718 1.080615 0.218 5 NCDN 0.740 1.079821 0.240 5GNAS 0.820 1.079212 0.320 5 CYFIP2 0.764 1.073980 0.264 5 PTPRK 0.7021.064478 0.202 5 GM1673 0.729 1.060925 0.229 5 HMGCS1 0.753 1.0606910.253 5 RTN1 0.800 1.055933 0.300 5 IGSF8 0.740 1.055664 0.240 5 SNRPN0.754 1.038591 0.254 5 THRA 0.772 1.020305 0.272 5 CHD3 0.753 1.0091070.253 5 GNB1 0.248 −1.603950 0.252 5 HMGN1 0.209 −1.639410 0.291 5UNC119 0.251 −1.776276 0.249 5 GNAT1 0.224 −1.788295 0.276 5 NEUROD10.273 −1.859046 0.227 5 RP1 0.233 −1.902106 0.267 5 PDE6B 0.237−1.916995 0.263 5 NRL 0.260 −1.922926 0.240 5 RCVRN 0.219 −1.9368050.281 5 ROM1 0.219 −2.012157 0.281 5 CNGA1 0.253 −2.027682 0.247 5 PDC0.180 −2.058464 0.320 5 PRPH2 0.189 −2.124104 0.311 5 RHO 0.175−2.140480 0.325 5 RS1 0.247 −2.154422 0.253 5 SAG 0.166 −2.161915 0.3345 NR2E3 0.249 −2.164806 0.251 5 GNGT1 0.160 −2.165857 0.340 5 RPGRIP10.244 −2.166108 0.256 5 SLC24A1 0.259 −2.174069 0.241 5 TULP1 0.195−2.237394 0.305 5 PDE6G 0.190 −2.267903 0.310 5 cluster no. 6 DE = 156NPNT 0.945 2.486780 0.445 6 ARL4C 0.938 2.467107 0.438 6 BHLHE22 0.9172.421611 0.417 6 CPLX2 0.942 2.362730 0.442 6 LPL 0.920 2.288892 0.420 6FILIP1L 0.897 2.194008 0.397 6 TKT 0.925 2.156892 0.425 6 NRXN2 0.9322.155552 0.432 6 SIX3 0.923 2.092244 0.423 6 SLIT2 0.911 2.087468 0.4116 SNHG11 0.935 2.050363 0.435 6 SLC6A1 0.885 1.911315 0.385 6 PAX6 0.8941.818176 0.394 6 PTN 0.892 1.811793 0.392 6 RBFOX1 0.853 1.801588 0.3536 DLGAP1 0.867 1.797541 0.367 6 GRIA2 0.898 1.738590 0.398 6 HBEGF 0.8121.719168 0.312 6 2900011O08RIK 0.863 1.692404 0.363 6 MEIS2 0.8871.620756 0.387 6 DTNBP1 0.839 1.601648 0.339 6 GAD1 0.851 1.596819 0.3516 ATP1B1 0.888 1.593981 0.388 6 ASAP1 0.841 1.587659 0.341 6 FEZ1 0.8231.583525 0.323 6 SPOCK3 0.826 1.577292 0.326 6 PCDH10 0.841 1.5528130.341 6 VSNL1 0.819 1.543639 0.319 6 NECAB1 0.807 1.542009 0.307 6 GAD20.800 1.511610 0.300 6 NRCAM 0.809 1.495982 0.309 6 GUCY1A3 0.8551.487265 0.355 6 ID4 0.791 1.477149 0.291 6 BASP1 0.849 1.466807 0.349 6PDE4B 0.803 1.466115 0.303 6 KCNIP1 0.807 1.464399 0.307 6 CXCL14 0.7711.455123 0.271 6 KCNC1 0.798 1.426647 0.298 6 RPH3A 0.835 1.420630 0.3356 FAM155A 0.804 1.420487 0.304 6 UCHL1 0.826 1.419570 0.326 6 DAPK10.786 1.411956 0.286 6 TTC3 0.887 1.400846 0.387 6 DPYSL4 0.796 1.3961610.296 6 GABBR2 0.746 1.395801 0.246 6 CCDC88B 0.779 1.375544 0.279 6SLC32A1 0.807 1.368830 0.307 6 C1QL1 0.772 1.360801 0.272 6 STMN2 0.8121.357504 0.312 6 ELAVL3 0.820 1.350815 0.320 6 RND3 0.779 1.347967 0.2796 GPM6A 0.835 1.344385 0.335 6 MEG3 0.875 1.342623 0.375 6 A030009H04RIK0.792 1.333141 0.292 6 ZFHX3 0.768 1.332239 0.268 6 RGS7BP 0.7691.324127 0.269 6 NDRG4 0.822 1.318106 0.322 6 RPS6KA4 0.748 1.3110230.248 6 ADARB1 0.798 1.302663 0.298 6 FRMD5 0.798 1.291730 0.298 6TUBB2A 0.825 1.288930 0.325 6 CTNND2 0.771 1.287176 0.271 6 CDK5R1 0.7881.279842 0.288 6 SV2A 0.826 1.279755 0.326 6 PRKCB 0.782 1.272974 0.2826 CACNG4 0.807 1.269842 0.307 6 UNC5D 0.741 1.260066 0.241 6 PRMT8 0.7531.258728 0.253 6 CACNA2D1 0.769 1.257272 0.269 6 GNG3 0.817 1.2511720.317 6 AUTS2 0.781 1.247146 0.281 6 STMN3 0.820 1.245952 0.320 6 FAIM20.772 1.244633 0.272 6 PNMAL2 0.804 1.239124 0.304 6 UBASH3B 0.7201.237485 0.220 6 RUNX1T1 0.768 1.222632 0.268 6 LRP8 0.761 1.2123090.261 6 STMN1 0.775 1.209730 0.275 6 6430548M08RIK 0.803 1.207834 0.3036 MPP6 0.761 1.206435 0.261 6 GPR123 0.736 1.204882 0.236 6 LHFPL2 0.7191.202920 0.219 6 COL6A1 0.747 1.199489 0.247 6 DHCR24 0.745 1.1950080.245 6 DUSP26 0.791 1.193817 0.291 6 ALCAM 0.712 1.183433 0.212 6INPP4B 0.736 1.177319 0.236 6 CLMN 0.701 1.175226 0.201 6 TSC22D1 0.8191.174524 0.319 6 SNRPN 0.792 1.174384 0.292 6 CELF4 0.835 1.173654 0.3356 HUNK 0.737 1.169421 0.237 6 TNC 0.723 1.167862 0.223 6 TFAP2A 0.7341.161882 0.234 6 RASAL2 0.740 1.156727 0.240 6 FGD6 0.741 1.156173 0.2416 ELAVL4 0.762 1.149500 0.262 6 GNG2 0.760 1.147975 0.260 6 LPHN3 0.7131.131097 0.213 6 PLCH1 0.734 1.129860 0.234 6 PCDH17 0.730 1.1275610.230 6 AI848285 0.704 1.120084 0.204 6 MYH10 0.779 1.111490 0.279 6TMEM191C 0.740 1.110693 0.240 6 GRIA4 0.752 1.109848 0.252 6 THRA 0.8011.109794 0.301 6 RASGRF1 0.710 1.104095 0.210 6 CHN1 0.759 1.0989000.259 6 CDC42EP4 0.706 1.091060 0.206 6 KIF5C 0.779 1.081707 0.279 6GAS7 0.763 1.080142 0.263 6 FSCN1 0.753 1.069197 0.253 6 6330403K07RIK0.713 1.065402 0.213 6 TAGLN3 0.766 1.056235 0.266 6 BC048943 0.7681.055497 0.268 6 ATP6V1G2 0.749 1.049524 0.249 6 GABRA3 0.738 1.0465000.238 6 HPCA 0.749 1.045573 0.249 6 FUT9 0.706 1.043984 0.206 6 CERS50.745 1.040396 0.245 6 FAM115A 0.777 1.038889 0.277 6 SFXN1 0.7261.037528 0.226 6 MLLT11 0.773 1.035476 0.273 6 SYNPR 0.758 1.0323180.258 6 CX3CL1 0.708 1.025068 0.208 6 MAPT 0.773 1.017509 0.273 6 DAAM10.744 1.012920 0.244 6 CMIP 0.752 1.011512 0.252 6 DKK3 0.836 1.0114270.336 6 IGSF8 0.733 1.003250 0.233 6 TENM4 0.703 1.002356 0.203 6 NSG20.752 1.001377 0.252 6 NRSN1 0.747 1.000763 0.247 6 CST3 0.293 −1.4658660.207 6 UNC119 0.276 −1.522563 0.224 6 HMGN1 0.218 −1.541634 0.282 6ROM1 0.257 −1.544670 0.243 6 GNB1 0.254 −1.581356 0.246 6 RPGRIP1 0.279−1.586358 0.221 6 NEUROD1 0.296 −1.619679 0.204 6 NRL 0.281 −1.6437320.219 6 CNGA1 0.281 −1.691412 0.219 6 PRPH2 0.220 −1.692216 0.280 6TULP1 0.227 −1.729834 0.273 6 NR2E3 0.278 −1.736613 0.222 6 RP1 0.256−1.749063 0.244 6 RS1 0.278 −1.760521 0.222 6 PDE6B 0.253 −1.7702640.247 6 PDE6G 0.227 −1.826063 0.273 6 SLC24A1 0.290 −1.831021 0.210 6SAG 0.180 −1.853215 0.320 6 RCVRN 0.234 −1.864629 0.266 6 GNAT1 0.222−1.882724 0.278 6 GNGT1 0.190 −1.891447 0.310 6 RHO 0.184 −1.9068230.316 6 PDC 0.188 −1.952769 0.312 6 cluster no. 7 DE = 164 CXCL14 0.9532.823229 0.453 7 CPLX2 0.965 2.782527 0.465 7 MAF 0.874 2.663386 0.374 7AI593442 0.929 2.533839 0.429 7 ID4 0.900 2.369125 0.400 7 LPL 0.9292.294283 0.429 7 GAD2 0.909 2.222806 0.409 7 NPNT 0.872 2.100390 0.372 7SNHG11 0.933 2.095661 0.433 7 SPOCK3 0.907 2.024941 0.407 7 PAX6 0.9061.900148 0.406 7 NRXN2 0.889 1.824692 0.389 7 GRIA2 0.907 1.794039 0.4077 NDRG4 0.889 1.706384 0.389 7 2900011O08RIK 0.866 1.702616 0.366 7DTNBP1 0.860 1.674204 0.360 7 C1QL1 0.836 1.656812 0.336 7 ASAP1 0.8481.646246 0.348 7 ATP1B1 0.904 1.636111 0.404 7 SIX3 0.866 1.635263 0.3667 SLC6A1 0.852 1.618210 0.352 7 FILIP1L 0.801 1.610463 0.301 7 HBEGF0.809 1.597965 0.309 7 PDE4B 0.838 1.597787 0.338 7 GUCY1A3 0.8641.582330 0.364 7 GAD1 0.851 1.579238 0.351 7 TNC 0.793 1.575202 0.293 7CRYBB3 0.732 1.574911 0.232 7 ADARB1 0.842 1.560392 0.342 7 MMP9 0.7441.559409 0.244 7 DNER 0.836 1.558484 0.336 7 SPARCL1 0.843 1.5502940.343 7 DDAH1 0.829 1.541302 0.329 7 DLGAP1 0.827 1.529146 0.327 7 UACA0.780 1.515731 0.280 7 MEIS2 0.864 1.513207 0.364 7 RBFOX1 0.8051.507393 0.305 7 TKT 0.856 1.505182 0.356 7 PCDH7 0.764 1.500815 0.264 7BHLHE22 0.799 1.499124 0.299 7 CLMN 0.781 1.470727 0.281 7 SLC32A1 0.8191.466542 0.319 7 BASP1 0.846 1.464820 0.346 7 ELMO1 0.787 1.457100 0.2877 CACNG4 0.843 1.450213 0.343 7 TUBB2A 0.849 1.445571 0.349 7 GNG2 0.8271.438293 0.327 7 GNG3 0.863 1.436732 0.363 7 DKK3 0.893 1.435250 0.393 7KCNA6 0.749 1.425320 0.249 7 NECAB1 0.792 1.419522 0.292 7 KCNAB1 0.7991.416904 0.299 7 ALDOC 0.847 1.409296 0.347 7 LMO4 0.743 1.409237 0.2437 6430548M08RIK 0.830 1.391242 0.330 7 FAM155A 0.818 1.381329 0.318 7PNMAL2 0.836 1.374099 0.336 7 KCNC1 0.817 1.373826 0.317 7 ARL4C 0.7831.370410 0.283 7 SCN3A 0.775 1.364878 0.275 7 SYT7 0.778 1.363974 0.2787 KIF5C 0.828 1.361801 0.328 7 TFAP2C 0.770 1.353114 0.270 7 FEZ1 0.7921.342916 0.292 7 PTN 0.817 1.337424 0.317 7 CELF4 0.871 1.326774 0.371 7TTC3 0.867 1.304565 0.367 7 CPNE6 0.779 1.303567 0.279 7 SV2A 0.8421.297245 0.342 7 CTSL 0.838 1.288834 0.338 7 MYH10 0.809 1.279803 0.3097 GABBR2 0.754 1.279715 0.254 7 FRMD5 0.810 1.278237 0.310 7 PAK3 0.7981.275646 0.298 7 PRKCB 0.771 1.274230 0.271 7 ELAVL3 0.811 1.2710940.311 7 ADARB2 0.740 1.270445 0.240 7 ARHGEF9 0.788 1.265682 0.288 7HUNK 0.784 1.259809 0.284 7 OGFRL1 0.809 1.255789 0.309 7 CPNE5 0.7461.249717 0.246 7 THRA 0.835 1.245177 0.335 7 KCNA1 0.753 1.239065 0.2537 KCNIP1 0.761 1.237502 0.261 7 SLIT2 0.767 1.237248 0.267 7 DPYSL40.786 1.232672 0.286 7 C1QL2 0.751 1.228475 0.251 7 THY1 0.774 1.2273680.274 7 PRUNE2 0.760 1.221889 0.260 7 ALCAM 0.713 1.207316 0.213 7DHCR24 0.776 1.189385 0.276 7 STMN3 0.826 1.187067 0.326 7 CD302 0.7061.182568 0.206 7 PRRT4 0.736 1.180616 0.236 7 PCSK2 0.749 1.162396 0.2497 DAPK1 0.751 1.145777 0.251 7 SEZ6L 0.717 1.139465 0.217 7 SFXN1 0.7571.133703 0.257 7 SYNPR 0.800 1.123498 0.300 7 VPS41 0.772 1.123170 0.2727 NSG2 0.798 1.120197 0.298 7 CCDC88B 0.730 1.113578 0.230 7 STMN2 0.7851.107607 0.285 7 MLLT11 0.797 1.107556 0.297 7 A030009H04RIK 0.7801.107031 0.280 7 VSNL1 0.752 1.103676 0.252 7 TAGLN3 0.802 1.1022300.302 7 ELAVL4 0.743 1.101000 0.243 7 LHFPL2 0.715 1.100922 0.215 7FRRS1L 0.713 1.100870 0.213 7 CERS5 0.750 1.098213 0.250 7 RND3 0.7261.095740 0.226 7 SNRPN 0.789 1.095115 0.289 7 GABRA3 0.732 1.0904410.232 7 PPFIBP1 0.706 1.080047 0.206 7 GAS7 0.770 1.079250 0.270 7INPP4B 0.710 1.078757 0.210 7 ATP6V1D 0.816 1.078276 0.316 7 FGD6 0.7211.073414 0.221 7 SPAG5 0.701 1.072308 0.201 7 ATP6V1G2 0.767 1.0684530.267 7 HPCA 0.758 1.064513 0.258 7 ARHGAP24 0.776 1.063113 0.276 7UBASH3B 0.720 1.061516 0.220 7 NAP1L5 0.804 1.060330 0.304 7 CACNG30.726 1.057606 0.226 7 MXRA7 0.781 1.057379 0.281 7 ADCY2 0.733 1.0554740.233 7 SYT11 0.792 1.054558 0.292 7 NPTX2 0.712 1.054379 0.212 7RPS6KA4 0.712 1.051053 0.212 7 UTRN 0.714 1.049219 0.214 7 BC0489430.793 1.047734 0.293 7 LPHN3 0.745 1.043811 0.245 7 MAPT 0.764 1.0369730.264 7 CTNND2 0.734 1.032653 0.234 7 AUTS2 0.749 1.032249 0.249 7SEPT11 0.742 1.032183 0.242 7 DAAM1 0.774 1.031598 0.274 7 PCP4L1 0.8011.029783 0.301 7 CACNB4 0.709 1.012396 0.209 7 MPP6 0.713 1.012265 0.2137 MARCKS 0.788 1.005504 0.288 7 GNB1 0.279 −1.346821 0.221 7 CST3 0.298−1.460907 0.202 7 HMGN1 0.231 −1.484621 0.269 7 ROM1 0.265 −1.5493540.235 7 NEUROD1 0.297 −1.576758 0.203 7 CNGA1 0.290 −1.593189 0.210 7RPGRIP1 0.294 −1.594350 0.206 7 RP1 0.270 −1.600478 0.230 7 TULP1 0.236−1.643426 0.264 7 NRL 0.284 −1.667221 0.216 7 PDE6G 0.239 −1.6757540.261 7 RCVRN 0.248 −1.702941 0.252 7 PDE6B 0.252 −1.720612 0.248 7SLC24A1 0.296 −1.738209 0.204 7 GNGT1 0.202 −1.745068 0.298 7 PRPH20.215 −1.759684 0.285 7 RS1 0.283 −1.786494 0.217 7 GNAT1 0.231−1.791925 0.269 7 PDC 0.196 −1.850697 0.304 7 SAG 0.181 −1.888991 0.3197 RHO 0.184 −1.898958 0.316 7 cluster no. 8 DE = 145 TAC2 0.842 3.1183770.342 8 TAC1 0.795 2.770889 0.295 8 STMN2 0.906 2.529338 0.406 8 GAP430.840 2.159206 0.340 8 NAP1L5 0.913 2.129231 0.413 8 ATP1B1 0.9162.091522 0.416 8 C1QL1 0.847 2.085033 0.347 8 CXCL14 0.750 2.0752830.250 8 MEG3 0.891 2.041950 0.391 8 SNHG11 0.891 2.017042 0.391 86330403K07RIK 0.824 1.993265 0.324 8 2900011O08RIK 0.866 1.975900 0.3668 UCHL1 0.861 1.947723 0.361 8 ELAVL2 0.762 1.912945 0.262 8 STMN3 0.8611.816792 0.361 8 CBLN2 0.711 1.800970 0.211 8 SPOCK3 0.809 1.7772510.309 8 NCAM2 0.788 1.760593 0.288 8 TUBB2A 0.861 1.711072 0.361 8TFAP2B 0.808 1.701796 0.308 8 SNCA 0.784 1.697970 0.284 8 SLC32A1 0.8091.663189 0.309 8 SCG2 0.824 1.651755 0.324 8 STMN4 0.809 1.645436 0.3098 CPNE5 0.789 1.634672 0.289 8 RTN1 0.852 1.593975 0.352 8 VSNL1 0.8061.570547 0.306 8 IMPACT 0.827 1.556732 0.327 8 SORCS1 0.773 1.5557930.273 8 GAD2 0.778 1.543560 0.278 8 BASP1 0.832 1.538785 0.332 8 CPLX20.799 1.530079 0.299 8 MEIS2 0.819 1.506350 0.319 8 GNG2 0.785 1.5031150.285 8 OXR1 0.753 1.492338 0.253 8 GNG3 0.817 1.478047 0.317 8 CELF40.859 1.464056 0.359 8 DNER 0.783 1.449112 0.283 8 TTC3 0.889 1.4249310.389 8 LSAMP 0.793 1.418734 0.293 8 NRXN2 0.815 1.414066 0.315 8 YWHAH0.794 1.410703 0.294 8 NECAB1 0.765 1.405108 0.265 8 SERPINE2 0.7011.401238 0.201 8 A030009H04RIK 0.788 1.397833 0.288 8 ZWINT 0.8081.388499 0.308 8 SLC6A1 0.797 1.385051 0.297 8 SYT11 0.816 1.3798770.316 8 GPRASP1 0.799 1.359056 0.299 8 4833424O15RIK 0.751 1.3553480.251 8 AI593442 0.713 1.339073 0.213 8 C1QL2 0.722 1.335015 0.222 8MLLT11 0.782 1.331374 0.282 8 GRIA2 0.831 1.326882 0.331 8 MARCKS 0.8271.322535 0.327 8 SYT6 0.714 1.321108 0.214 8 NRSN1 0.757 1.319183 0.2578 TFAP2A 0.713 1.313087 0.213 8 KIF5C 0.784 1.312896 0.284 8 SYN2 0.7111.309829 0.211 8 TENM1 0.730 1.298569 0.230 8 EPB4.1L4A 0.713 1.2965850.213 8 PAX6 0.784 1.290939 0.284 8 NDN 0.805 1.284206 0.305 8 GPM6A0.815 1.282328 0.315 8 FXYD6 0.740 1.268025 0.240 8 GNAS 0.849 1.2675170.349 8 SYT7 0.738 1.267166 0.238 8 SNRPN 0.765 1.264829 0.265 8 SPOCK20.771 1.263568 0.271 8 PNMAL2 0.771 1.259210 0.271 8 MAPT 0.770 1.2449830.270 8 MYT1L 0.752 1.241489 0.252 8 HSP90AB1 0.873 1.236035 0.373 8BEX2 0.803 1.234094 0.303 8 NDRG4 0.787 1.229175 0.287 8 TKT 0.7471.227076 0.247 8 GAD1 0.734 1.218844 0.234 8 TCEAL5 0.748 1.204026 0.2488 TENM4 0.719 1.203590 0.219 8 NSG2 0.743 1.203252 0.243 8 SYNGR3 0.7351.190339 0.235 8 YWHAG 0.770 1.184824 0.270 8 GRIA3 0.714 1.181042 0.2148 FSTL5 0.737 1.177141 0.237 8 NSG1 0.744 1.176358 0.244 8 SPARCL1 0.7621.174529 0.262 8 TMX4 0.753 1.169642 0.253 8 REEP5 0.734 1.166393 0.2348 SYNPR 0.769 1.155357 0.269 8 TUBA1A 0.793 1.148357 0.293 8 NGFRAP10.765 1.133358 0.265 8 TMSB10 0.770 1.132117 0.270 8 CACNA2D2 0.7231.117231 0.223 8 CALM2 0.801 1.114501 0.301 8 RBFOX1 0.712 1.1142990.212 8 PRKAR1B 0.731 1.103338 0.231 8 GM1673 0.720 1.098747 0.220 8SERINC1 0.791 1.098697 0.291 8 SV2A 0.782 1.095818 0.282 8 APP 0.7481.089714 0.248 8 ZCCHC18 0.740 1.081228 0.240 8 CALM3 0.773 1.0715030.273 8 GPRASP2 0.738 1.069399 0.238 8 RAB6B 0.736 1.066369 0.236 8GRIA4 0.729 1.065619 0.229 8 LRRC4C 0.701 1.059002 0.201 8 KIF5A 0.7091.050514 0.209 8 DTNBP1 0.720 1.042708 0.220 8 RAB6A 0.752 1.0401960.252 8 CD200 0.709 1.038274 0.209 8 CHGA 0.752 1.036109 0.252 8 KIF3A0.743 1.036025 0.243 8 CDK5R1 0.735 1.035358 0.235 8 ACOT7 0.7151.035198 0.215 8 CACNG4 0.739 1.032652 0.239 8 TPM1 0.732 1.026026 0.2328 OLFM1 0.705 1.021312 0.205 8 ELAVL3 0.744 1.019574 0.244 8 KIFAP30.762 1.019268 0.262 8 D3BWG0562E 0.717 1.014043 0.217 8 EPB4.1 0.292−1.765515 0.208 8 GNB1 0.237 −1.768119 0.263 8 NEUROD1 0.267 −1.8030150.233 8 HMGN1 0.185 −1.892020 0.315 8 AIPL1 0.297 −1.980059 0.203 8UNC119 0.225 −2.011676 0.275 8 RP1 0.218 −2.092140 0.282 8 NR2E3 0.243−2.160752 0.257 8 NRL 0.239 −2.167337 0.261 8 CNGA1 0.229 −2.2336350.271 8 ROM1 0.197 −2.307381 0.303 8 PDE6B 0.210 −2.319014 0.290 8RPGRIP1 0.231 −2.350954 0.269 8 PRPH2 0.170 −2.376545 0.330 8 PDE6G0.187 −2.377062 0.313 8 RS1 0.230 −2.386965 0.270 8 SLC24A1 0.240−2.450802 0.260 8 GNAT1 0.176 −2.480741 0.324 8 SAG 0.140 −2.4818920.360 8 RCVRN 0.187 −2.497213 0.313 8 RHO 0.146 −2.536232 0.354 8 GNGT10.133 −2.654791 0.367 8 TULP1 0.165 −2.680406 0.335 8 PDC 0.144−2.702042 0.356 8 cluster no. 9 DE = 145 TFAP2B 0.913 2.692482 0.413 9ATP1B1 0.940 2.501021 0.440 9 C1QL1 0.921 2.473758 0.421 9 CBLN2 0.9032.412823 0.403 9 MARCKS 0.932 2.121128 0.432 9 SNHG11 0.938 2.1076670.438 9 OLFM3 0.817 2.099649 0.317 9 FILIP1L 0.824 2.028323 0.324 9SLC6A1 0.888 1.981368 0.388 9 NRXN2 0.882 1.930215 0.382 9 GAD1 0.8881.921463 0.388 9 CACNA2D2 0.851 1.807684 0.351 9 CHGA 0.879 1.7933440.379 9 C1QL2 0.838 1.774575 0.338 9 BASP1 0.866 1.743280 0.366 9 GAP430.818 1.741537 0.318 9 IGFBP2 0.769 1.726564 0.269 9 TBX3 0.788 1.6996900.288 9 TFAP2A 0.806 1.692081 0.306 9 SYT7 0.773 1.670252 0.273 9 LRRN30.806 1.657383 0.306 9 ADARB1 0.839 1.646173 0.339 9 UCHL1 0.8641.644685 0.364 9 PAX6 0.862 1.638791 0.362 9 MEG3 0.907 1.603859 0.407 9DTNBP1 0.818 1.591595 0.318 9 6430548M08RIK 0.838 1.587475 0.338 9ELAVL3 0.838 1.578197 0.338 9 KCNAB1 0.817 1.568133 0.317 9 GNG2 0.7971.564002 0.297 9 NPTX2 0.756 1.555687 0.256 9 AI593442 0.796 1.5449860.296 9 CELF4 0.886 1.538491 0.386 9 FRMD5 0.828 1.522471 0.328 9 EEF1E10.810 1.514397 0.310 9 WBSCR17 0.788 1.491530 0.288 9 PDE3A 0.7611.485254 0.261 9 RGS8 0.793 1.484142 0.293 9 ELOVL6 0.784 1.477738 0.2849 MEIS2 0.840 1.475665 0.340 9 GNG3 0.848 1.474628 0.348 9 SLC32A1 0.8151.466099 0.315 9 ID4 0.756 1.412435 0.256 9 SYNPR 0.826 1.410647 0.326 9PRKAR2B 0.775 1.395009 0.275 9 LIN7A 0.849 1.394313 0.349 9 MAPT 0.8081.376944 0.308 9 GABRA3 0.779 1.365007 0.279 9 RYR2 0.766 1.360686 0.2669 NDRG4 0.822 1.358598 0.322 9 PRKCE 0.808 1.355495 0.308 9 LOXL2 0.7291.349178 0.229 9 ATP2B4 0.739 1.348942 0.239 9 NETO2 0.745 1.3114990.245 9 ALDOC 0.789 1.306160 0.289 9 WDR1 0.781 1.305461 0.281 9 GRIA30.760 1.295841 0.260 9 PHACTR3 0.773 1.289285 0.273 9 FABP3 0.7441.276022 0.244 9 TUBB2A 0.815 1.274976 0.315 9 LSAMP 0.793 1.2726500.293 9 SLC6A11 0.755 1.267563 0.255 9 DLGAP1 0.769 1.263219 0.269 9NAV1 0.788 1.259667 0.288 9 CPNE6 0.754 1.258456 0.254 9 TMEM191C 0.7491.258008 0.249 9 SOX5 0.723 1.251003 0.223 9 CPLX3 0.800 1.243626 0.3009 BC048943 0.813 1.230504 0.313 9 SEMA6A 0.748 1.229853 0.248 9 CCDC88B0.726 1.229532 0.226 9 STMN3 0.814 1.228264 0.314 9 CLMP 0.711 1.2278890.211 9 HABP4 0.785 1.219840 0.285 9 KIF5C 0.805 1.219184 0.305 9MARCKSL1 0.788 1.217008 0.288 9 VSNL1 0.757 1.216340 0.257 9 LHX9 0.7211.197847 0.221 9 GABRG2 0.752 1.191982 0.252 9 ARHGAP20 0.723 1.1912300.223 9 KCNA1 0.724 1.188659 0.224 9 ATP2B1 0.807 1.184449 0.307 9 TPM10.770 1.181575 0.270 9 SV2A 0.806 1.181132 0.306 9 NSG1 0.782 1.1785000.282 9 TTC3 0.842 1.174244 0.342 9 NAP1L5 0.796 1.164618 0.296 9A030009H04RIK 0.780 1.164223 0.280 9 DPYSL2 0.770 1.157861 0.270 9 THY10.740 1.146696 0.240 9 GPRASP1 0.810 1.145215 0.310 9 SPOCK3 0.7671.142882 0.267 9 MLLT11 0.780 1.141012 0.280 9 RTN1 0.809 1.140966 0.3099 CHD3 0.776 1.135535 0.276 9 HSD17B12 0.790 1.135531 0.290 9 RUNX1T10.759 1.130153 0.259 9 ITM2C 0.799 1.124268 0.299 9 HSP90AB1 0.8421.112076 0.342 9 SRGAP3 0.742 1.110121 0.242 9 GNAS 0.841 1.102581 0.3419 CHGB 0.803 1.091361 0.303 9 NSG2 0.757 1.091212 0.257 9 OXR1 0.7571.084787 0.257 9 SYT11 0.778 1.081871 0.278 9 CYFIP2 0.748 1.0771680.248 9 ZEB2 0.742 1.075057 0.242 9 DPP6 0.743 1.072735 0.243 9 CD470.784 1.071126 0.284 9 IMPACT 0.764 1.070542 0.264 9 HSPA12A 0.7551.068676 0.255 9 SH3BP5 0.716 1.067537 0.216 9 RBFOX2 0.741 1.0631770.241 9 TPPP 0.713 1.062940 0.213 9 SNCB 0.789 1.062761 0.289 9 COL23A10.760 1.056620 0.260 9 CALM3 0.777 1.053213 0.277 9 TKT 0.775 1.0514750.275 9 EPB4.1L4A 0.701 1.043584 0.201 9 FBXO32 0.705 1.032729 0.205 9GM1673 0.732 1.019184 0.232 9 FAM115A 0.749 1.016772 0.249 9 ECE1 0.7041.007563 0.204 9 YWHAG 0.760 1.007454 0.260 9 GNB1 0.254 −1.559334 0.2469 HMGN1 0.215 −1.594457 0.285 9 RP1 0.248 −1.629751 0.252 9 UNC119 0.267−1.642090 0.233 9 NR2E3 0.271 −1.829500 0.229 9 CNGA1 0.268 −1.8709630.232 9 TULP1 0.211 −1.901678 0.289 9 ROM1 0.231 −1.909354 0.269 9RPGRIP1 0.259 −1.928781 0.241 9 NRL 0.257 −1.975762 0.243 9 PRPH2 0.194−1.981809 0.306 9 SLC24A1 0.266 −1.993990 0.234 9 PDE6G 0.205 −2.0451030.295 9 RS1 0.259 −2.057027 0.241 9 PDE6B 0.227 −2.071134 0.273 9 RCVRN0.215 −2.076463 0.285 9 GNAT1 0.204 −2.091716 0.296 9 SAG 0.157−2.182196 0.343 9 PDC 0.170 −2.185807 0.330 9 RHO 0.163 −2.201967 0.3379 GNGT1 0.163 −2.222527 0.337 9 cluster no. 10 DE = 120 VIP 0.7673.830134 0.267 10 CARTPT 0.830 2.551837 0.330 10 CBLN2 0.897 2.3718610.397 10 SLC6A1 0.912 2.250550 0.412 10 GABRA2 0.841 2.143980 0.341 10SNHG11 0.945 2.134197 0.445 10 NR4A2 0.835 2.098562 0.335 10 NNAT 0.8002.051593 0.300 10 CBLN4 0.727 2.045730 0.227 10 TFAP2B 0.876 2.0243790.376 10 GAD1 0.855 1.986823 0.355 10 6430548M08RIK 0.876 1.940600 0.37610 NAP1L5 0.892 1.812106 0.392 10 NRSN1 0.822 1.779217 0.322 10 GRIA30.750 1.767426 0.250 10 MEG3 0.912 1.766291 0.412 10 SYT6 0.739 1.7221860.239 10 GAD2 0.795 1.711410 0.295 10 CELF4 0.909 1.695323 0.409 102900011O08RIK 0.847 1.663963 0.347 10 STMN4 0.794 1.657861 0.294 10ATP1B1 0.885 1.613084 0.385 10 RAB3C 0.824 1.612804 0.324 10 CACNA2D20.800 1.543215 0.300 10 TKT 0.827 1.542467 0.327 10 MARCKS 0.8611.534529 0.361 10 RNF220 0.820 1.519204 0.320 10 PAX6 0.826 1.4946660.326 10 GAP43 0.736 1.494533 0.236 10 ELAVL3 0.829 1.476012 0.329 10LRRTM1 0.745 1.466343 0.245 10 4833424O15RIK 0.735 1.455809 0.235 10NDRG4 0.835 1.451943 0.335 10 SLC32A1 0.824 1.449471 0.324 10 HS6ST20.717 1.430399 0.217 10 SYT1 0.914 1.419385 0.414 10 GNG2 0.765 1.3998220.265 10 ZCCHC12 0.711 1.393990 0.211 10 UCHL1 0.797 1.376379 0.297 10HLF 0.815 1.374388 0.315 10 VSNL1 0.745 1.358259 0.245 10 GNG3 0.8261.316743 0.326 10 A030009H04RIK 0.787 1.309649 0.287 10 TTC3 0.8661.305950 0.366 10 BASP1 0.796 1.302431 0.296 10 GPM6A 0.847 1.3012110.347 10 SYNPR 0.808 1.298962 0.308 10 TAGLN3 0.796 1.289770 0.296 10DLGAP1 0.744 1.260355 0.244 10 GPRASP1 0.802 1.252102 0.302 10 SLC6A110.734 1.251426 0.234 10 KIF5C 0.790 1.248227 0.290 10 NDN 0.799 1.2096170.299 10 ELAVL4 0.715 1.195958 0.215 10 GABRG2 0.766 1.191704 0.266 10NSG2 0.748 1.180941 0.248 10 RUNX1T1 0.711 1.177126 0.211 10 PNMAL20.766 1.175260 0.266 10 NSG1 0.771 1.173586 0.271 10 CHD5 0.711 1.1688340.211 10 SV2A 0.812 1.167811 0.312 10 GABRA3 0.702 1.163683 0.202 10BEX1 0.754 1.160868 0.254 10 GRM1 0.704 1.158057 0.204 10 NGFRAP1 0.7931.157896 0.293 10 SPOCK3 0.730 1.139949 0.230 10 6330403K07RIK 0.7231.136823 0.223 10 IMPACT 0.756 1.136763 0.256 10 GRIA4 0.705 1.1340380.205 10 STMN2 0.719 1.126131 0.219 10 MAPT 0.773 1.125378 0.273 10MARCKSL1 0.764 1.124830 0.264 10 PAK3 0.730 1.118891 0.230 10 ZCCHC180.765 1.116777 0.265 10 CACNG3 0.702 1.116442 0.202 10 GRIA2 0.7881.114119 0.288 10 YWHAH 0.753 1.111748 0.253 10 SYT4 0.745 1.1112490.245 10 TCEAL5 0.733 1.104752 0.233 10 SYT11 0.783 1.101958 0.283 10STMN3 0.750 1.099315 0.250 10 NRXN2 0.768 1.098278 0.268 10 SLC22A170.754 1.090749 0.254 10 LY6H 0.721 1.080063 0.221 10 FXYD6 0.7271.064334 0.227 10 FAM115A 0.734 1.055395 0.234 10 GM1673 0.723 1.0552830.223 10 GNAS 0.822 1.047020 0.322 10 APP 0.755 1.039216 0.255 10 CACNG40.730 1.037850 0.230 10 ZWINT 0.752 1.036807 0.252 10 TMEM130 0.7011.032886 0.201 10 D3BWG0562E 0.716 1.025310 0.216 10 LIN7A 0.7751.021321 0.275 10 MLLT11 0.750 1.017950 0.250 10 RTN1 0.801 1.0165980.301 10 BEX2 0.797 1.008599 0.297 10 SNRPN 0.753 1.000211 0.253 10 GNB10.252 −1.543483 0.248 10 HMGN1 0.216 −1.579673 0.284 10 CNGA1 0.274−1.673428 0.226 10 UNC119 0.245 −1.746828 0.255 10 NRL 0.262 −1.7960010.238 10 NEUROD1 0.277 −1.806110 0.223 10 NR2E3 0.256 −1.883207 0.244 10PDE6B 0.229 −1.927154 0.271 10 ROM1 0.218 −1.942172 0.282 10 RP1 0.231−1.972704 0.269 10 TULP1 0.205 −1.993368 0.295 10 PRPH2 0.192 −2.0090750.308 10 RCVRN 0.217 −2.034673 0.283 10 PDE6G 0.197 −2.035379 0.303 10GNAT1 0.205 −2.035699 0.295 10 SLC24A1 0.258 −2.054582 0.242 10 GNGT10.164 −2.075342 0.336 10 RS1 0.255 −2.087538 0.245 10 RPGRIP1 0.240−2.097159 0.260 10 SAG 0.155 −2.153542 0.345 10 PDC 0.169 −2.1785520.331 10 RHO 0.160 −2.190204 0.340 10 cluster no. 11 DE = 111 SLC6A10.931 2.333915 0.431 11 PCDH17 0.863 2.136196 0.363 11 DNER 0.8852.116049 0.385 11 ID4 0.806 2.095898 0.306 11 TFAP2B 0.830 2.0831320.330 11 SNHG11 0.930 2.057025 0.430 11 SYT7 0.813 2.030645 0.313 11ATP1B1 0.914 1.999429 0.414 11 GAD1 0.851 1.909032 0.351 11 MEIS2 0.8771.853622 0.377 11 SYNPR 0.879 1.830302 0.379 11 SPARCL1 0.787 1.8092690.287 11 FRMD5 0.838 1.786740 0.338 11 TKT 0.863 1.751565 0.363 11 GRIA20.861 1.721134 0.361 11 AI848285 0.734 1.720216 0.234 11 GFRA1 0.7531.715834 0.253 11 MEG3 0.905 1.705098 0.405 11 NDRG4 0.850 1.6875780.350 11 NAP1L5 0.848 1.685433 0.348 11 PAX6 0.822 1.680286 0.322 11ESRRG 0.754 1.614605 0.254 11 PTPRT 0.714 1.601504 0.214 11 NRXN2 0.8251.588975 0.325 11 6430548M08RIK 0.813 1.574957 0.313 11 ADARB1 0.8011.564237 0.301 11 ELAVL3 0.828 1.553803 0.328 11 BASP1 0.839 1.5451730.339 11 GAD2 0.764 1.519852 0.264 11 ZFHX3 0.783 1.488418 0.283 11GABRG2 0.811 1.485814 0.311 11 CACNA2D2 0.763 1.479819 0.263 11 VSNL10.757 1.475157 0.257 11 SV2A 0.838 1.462079 0.338 11 CELF4 0.8671.458085 0.367 11 DPP6 0.778 1.451701 0.278 11 DUSP26 0.785 1.4493440.285 11 CHN2 0.719 1.444832 0.219 11 TSHZ1 0.701 1.403224 0.201 11DYNC1I1 0.719 1.398013 0.219 11 DLGAP1 0.763 1.388125 0.263 11 SLC32A10.776 1.339618 0.276 11 APP 0.827 1.335361 0.327 11 VSTM2B 0.7081.333834 0.208 11 2900011O08RIK 0.788 1.318652 0.288 11 LDHB 0.7661.315407 0.266 11 SPOCK3 0.772 1.315060 0.272 11 TTC3 0.855 1.3089930.355 11 ELAVL4 0.723 1.307010 0.223 11 CYGB 0.743 1.300364 0.243 11NRSN1 0.756 1.299498 0.256 11 GNG3 0.804 1.280594 0.304 11 NRXN1 0.7251.273732 0.225 11 KIF5C 0.766 1.262018 0.266 11 TMEM191C 0.728 1.2509650.228 11 RIT2 0.737 1.246639 0.237 11 PCP4 0.706 1.237709 0.206 11 RGS80.709 1.234002 0.209 11 PNMAL2 0.770 1.228431 0.270 11 STMN3 0.8071.225751 0.307 11 FABP3 0.704 1.222551 0.204 11 CALY 0.729 1.2206550.229 11 CHN1 0.749 1.219803 0.249 11 A030009H04RIK 0.740 1.205040 0.24011 SIX6 0.711 1.201685 0.211 11 DKK3 0.804 1.196969 0.304 11 GPRASP10.788 1.175368 0.288 11 TMX4 0.746 1.167458 0.246 11 DHCR24 0.7021.159663 0.202 11 SYT11 0.750 1.142552 0.250 11 NSG2 0.709 1.1244890.209 11 RPH3A 0.713 1.118261 0.213 11 AUTS2 0.710 1.102486 0.210 11GPM6A 0.778 1.101162 0.278 11 CYFIP2 0.731 1.094488 0.231 11 CD47 0.7381.094214 0.238 11 GRIA4 0.709 1.066388 0.209 11 PBX1 0.760 1.0640810.260 11 PRKACB 0.721 1.048412 0.221 11 SYT4 0.708 1.043194 0.208 11MAPT 0.729 1.037623 0.229 11 SERINC1 0.789 1.037343 0.289 11 GABRA10.728 1.031688 0.228 11 TAGLN3 0.715 1.030901 0.215 11 ZWINT 0.7301.019322 0.230 11 KCNC1 0.722 1.018621 0.222 11 CHD3 0.705 1.0177700.205 11 ATP6V1G2 0.717 1.016268 0.217 11 SNCB 0.769 1.015930 0.269 11HMGN1 0.215 −1.563282 0.285 11 GNB1 0.242 −1.670947 0.258 11 NEUROD10.282 −1.681634 0.218 11 UNC119 0.251 −1.717318 0.249 11 NR2E3 0.268−1.718845 0.232 11 CNGA1 0.260 −1.814289 0.240 11 ROM1 0.231 −1.8332840.269 11 SLC24A1 0.277 −1.869445 0.223 11 RPGRIP1 0.248 −1.918559 0.25211 TULP1 0.204 −1.929248 0.296 11 RS1 0.257 −1.929959 0.243 11 RP1 0.229−1.939595 0.271 11 NRL 0.255 −1.968506 0.245 11 PRPH2 0.194 −1.9894650.306 11 PDE6B 0.225 −2.074086 0.275 11 RCVRN 0.214 −2.090257 0.286 11GNAT1 0.200 −2.097595 0.300 11 RHO 0.164 −2.136073 0.336 11 PDE6G 0.195−2.169314 0.305 11 PDC 0.164 −2.204122 0.336 11 SAG 0.152 −2.2361810.348 11 GNGT1 0.154 −2.283434 0.346 11 cluster no. 12 DE = 68 SLC6A10.874 2.180099 0.374 12 CBLN2 0.754 1.928113 0.254 12 PAX6 0.8281.886874 0.328 12 TKT 0.826 1.848995 0.326 12 SNHG11 0.868 1.8282750.368 12 TFAP2B 0.804 1.768165 0.304 12 NAP1L5 0.824 1.752147 0.324 12GAD1 0.768 1.707274 0.268 12 PCDH10 0.714 1.651388 0.214 12 SIX3 0.7141.622442 0.214 12 MEG3 0.863 1.616915 0.363 12 CELF4 0.845 1.5833060.345 12 ATP1B1 0.822 1.555753 0.322 12 SYNPR 0.745 1.536495 0.245 122900011O08RIK 0.770 1.510272 0.270 12 CACNG4 0.753 1.474837 0.253 12FRMD5 0.749 1.458548 0.249 12 MEIS2 0.722 1.457447 0.222 12 ZFHX3 0.7121.448061 0.212 12 BASP1 0.781 1.447063 0.281 12 RPH3A 0.721 1.4220910.221 12 GRIA2 0.795 1.402898 0.295 12 GUCY1A3 0.713 1.393783 0.213 12DPYSL4 0.718 1.360517 0.218 12 PNMAL2 0.744 1.343839 0.244 12 RUNX1T10.713 1.335288 0.213 12 ELAVL3 0.748 1.329163 0.248 12 RAB3C 0.7101.324800 0.210 12 NRSN1 0.721 1.306849 0.221 12 UCHL1 0.736 1.3007850.236 12 TTC3 0.832 1.295748 0.332 12 ADARB1 0.723 1.277937 0.223 12GNG3 0.765 1.263270 0.265 12 NDRG4 0.744 1.253376 0.244 12 A030009H04RIK0.706 1.252601 0.206 12 SV2A 0.785 1.240701 0.285 12 DUSP26 0.7151.211692 0.215 12 APC 0.753 1.150275 0.253 12 GPRASP1 0.737 1.1478360.237 12 GPM6A 0.752 1.141256 0.252 12 TMX4 0.707 1.122604 0.207 12 RTN10.749 1.119089 0.249 12 NRXN2 0.709 1.113600 0.209 12 LDHB 0.7051.097431 0.205 12 NGFRAP1 0.709 1.075985 0.209 12 NDN 0.708 1.0618560.208 12 BEX2 0.754 1.041420 0.254 12 MARCKS 0.731 1.019699 0.231 12HMGN1 0.250 −1.195481 0.250 12 GNB1 0.268 −1.266009 0.232 12 RP1 0.280−1.277829 0.220 12 NR2E3 0.296 −1.336009 0.204 12 RPGRIP1 0.290−1.341698 0.210 12 RCVRN 0.261 −1.376084 0.239 12 NRL 0.292 −1.3930050.208 12 UNC119 0.266 −1.397189 0.234 12 PRPH2 0.232 −1.433849 0.268 12TULP1 0.238 −1.438510 0.262 12 ROM1 0.258 −1.441911 0.242 12 RS1 0.292−1.451877 0.208 12 PDE6B 0.265 −1.484310 0.235 12 GNAT1 0.238 −1.5165900.262 12 CNGA1 0.285 −1.525788 0.215 12 RHO 0.205 −1.537955 0.295 12 SAG0.196 −1.550193 0.304 12 PDC 0.212 −1.561538 0.288 12 GNGT1 0.204−1.581874 0.296 12 PDE6G 0.228 −1.637557 0.272 12 cluster no. 13 DE =163 SCG2 0.963 2.746757 0.463 13 LAMP5 0.949 2.686845 0.449 13 TFAP2B0.960 2.600604 0.460 13 SLC6A1 0.939 2.455520 0.439 13 GAD1 0.9102.214303 0.410 13 RASGRP1 0.917 2.098422 0.417 13 CBLN2 0.897 2.0197540.397 13 GAP43 0.868 2.007008 0.368 13 GRIA3 0.912 1.939880 0.412 13SNHG11 0.940 1.931816 0.440 13 PCDH17 0.888 1.870311 0.388 13 CBLN10.848 1.804900 0.348 13 TAGLN3 0.895 1.804474 0.395 13 GM2694 0.8361.763564 0.336 13 TFAP2A 0.867 1.742085 0.367 13 SPARCL1 0.896 1.7275350.396 13 PDGFRA 0.838 1.722897 0.338 13 RAB3C 0.902 1.716234 0.402 13NAP1L5 0.901 1.703198 0.401 13 GUCY1A3 0.893 1.681253 0.393 13 CELF40.919 1.676011 0.419 13 SPOCK3 0.903 1.642174 0.403 13 LNX1 0.8631.623297 0.363 13 SEMA3A 0.816 1.615345 0.316 13 LRRTM1 0.867 1.6023510.367 13 NSG1 0.838 1.594951 0.338 13 TMEM179 0.841 1.593475 0.341 13FRMD5 0.886 1.585843 0.386 13 ATP1B1 0.912 1.585191 0.412 13 AI5934420.845 1.575313 0.345 13 GJC1 0.793 1.560209 0.293 13 CYGB 0.879 1.5195980.379 13 PHLDA1 0.818 1.515132 0.318 13 MEG3 0.909 1.503058 0.409 13DPP6 0.886 1.502219 0.386 13 DKK3 0.892 1.481844 0.392 13 KCNIP1 0.8551.481648 0.355 13 NDRG4 0.878 1.480199 0.378 13 SYN2 0.844 1.4777260.344 13 SLC32A1 0.856 1.462162 0.356 13 ELAVL4 0.818 1.457094 0.318 13ISOC1 0.759 1.449689 0.259 13 ALDOC 0.874 1.444666 0.374 13 FNBP1L 0.8291.440875 0.329 13 ELAVL3 0.862 1.418171 0.362 13 SV2A 0.891 1.4161600.391 13 GRIA4 0.865 1.408494 0.365 13 RGS17 0.785 1.404754 0.285 13UCHL1 0.837 1.390501 0.337 13 NRSN1 0.875 1.376384 0.375 13 PTPRM 0.8031.366832 0.303 13 NSG2 0.858 1.361192 0.358 13 DNM3 0.890 1.359611 0.39013 CLMP 0.784 1.357481 0.284 13 GNG3 0.838 1.348245 0.338 132900011O08RIK 0.845 1.338735 0.345 13 LHX9 0.815 1.337030 0.315 13 VAMP40.854 1.335530 0.354 13 CAMKV 0.815 1.331781 0.315 13 DTNBP1 0.8461.329320 0.346 13 GAD2 0.805 1.326719 0.305 13 ANK3 0.838 1.323306 0.33813 BASP1 0.865 1.316675 0.365 13 FGF10 0.748 1.308488 0.248 13 STMN30.861 1.296175 0.361 13 FUT9 0.783 1.296115 0.283 13 IMPACT 0.8421.295463 0.342 13 SYT4 0.862 1.289100 0.362 13 PAX6 0.864 1.287430 0.36413 TENM1 0.790 1.285335 0.290 13 MAPT 0.830 1.283527 0.330 13 RGS8 0.8231.279287 0.323 13 NECAB1 0.789 1.268538 0.289 13 GRM1 0.751 1.2530730.251 13 CALN1 0.773 1.247262 0.273 13 CACNA2D2 0.838 1.237957 0.338 13ZWINT 0.860 1.220447 0.360 13 RBFOX2 0.793 1.217025 0.293 13 OPCML 0.7721.212407 0.272 13 E130218I03RIK 0.871 1.204019 0.371 13 LMO4 0.8031.203676 0.303 13 ATP6V1G2 0.820 1.202503 0.320 13 GABRA2 0.761 1.2024760.261 13 MARCKS 0.867 1.199734 0.367 13 TCEAL5 0.795 1.195481 0.295 13SYNPR 0.800 1.181298 0.300 13 GABRA3 0.767 1.176700 0.267 13 MLLT110.810 1.174360 0.310 13 VSTM2L 0.775 1.171942 0.275 13 A030009H04RIK0.799 1.167220 0.299 13 ASPH 0.848 1.166139 0.348 13 SNRPN 0.8191.165623 0.319 13 DNER 0.814 1.158918 0.314 13 TMEM191C 0.811 1.1561700.311 13 PRKAR1A 0.858 1.150894 0.358 13 TTC3 0.867 1.150786 0.367 13HPGD 0.742 1.145794 0.242 13 SH3BGRL 0.818 1.143089 0.318 13 TUBB2A0.858 1.142518 0.358 13 ITM2C 0.855 1.132688 0.355 13 DLG2 0.7551.127546 0.255 13 EPB4.1L4A 0.758 1.123112 0.258 13 SLC6A5 0.7571.122854 0.257 13 LSAMP 0.790 1.119316 0.290 13 SLC24A2 0.751 1.1171280.251 13 RUNX1T1 0.796 1.116379 0.296 13 SNCB 0.829 1.114629 0.329 13CRABP1 0.723 1.112187 0.223 13 MARCKSL1 0.786 1.109417 0.286 13 NGFRAP10.841 1.105288 0.341 13 GRIA2 0.843 1.099977 0.343 13 LDHB 0.8361.091893 0.336 13 6330403K07RIK 0.716 1.089339 0.216 13 RTN1 0.8351.088449 0.335 13 CPLX3 0.837 1.084019 0.337 13 PAK3 0.780 1.0836270.280 13 GNAS 0.836 1.081193 0.336 13 NRXN2 0.809 1.081039 0.309 13 PJA20.823 1.077566 0.323 13 VSNL1 0.759 1.077335 0.259 13 PRKCE 0.8081.072516 0.308 13 TMX4 0.787 1.065684 0.287 13 SYT11 0.821 1.0646470.321 13 CFL1 0.829 1.063733 0.329 13 STEAP2 0.779 1.060304 0.279 13ABAT 0.753 1.048614 0.253 13 GM1673 0.772 1.046935 0.272 136430548M08RIK 0.807 1.045290 0.307 13 CALM1 0.890 1.044110 0.390 13VSTM2A 0.755 1.039415 0.255 13 SERP2 0.757 1.039018 0.257 13 DLGAP10.758 1.032184 0.258 13 WDR1 0.775 1.031819 0.275 13 BEX2 0.825 1.0309740.325 13 GRIK2 0.727 1.028371 0.227 13 LINGO1 0.726 1.021154 0.226 13HSP90AB1 0.835 1.017052 0.335 13 NCALD 0.744 1.014432 0.244 13 NDN 0.8031.013667 0.303 13 YWHAH 0.767 1.006233 0.267 13 PIP4K2A 0.728 1.0062240.228 13 GNB1 0.250 −1.654835 0.250 13 HMGN1 0.219 −1.661459 0.281 13UNC119 0.271 −1.736377 0.229 13 NR2E3 0.259 −1.757150 0.241 13 ROM10.226 −2.024256 0.274 13 RS1 0.250 −2.076870 0.250 13 RP1 0.229−2.081436 0.271 13 NRL 0.264 −2.089632 0.236 13 NEUROD1 0.268 −2.0942200.232 13 PDC 0.174 −2.144862 0.326 13 PDE6B 0.225 −2.217360 0.275 13SLC24A1 0.253 −2.275124 0.247 13 CNGA1 0.251 −2.284090 0.249 13 GNAT10.190 −2.284263 0.310 13 PRPH2 0.185 −2.326461 0.315 13 RCVRN 0.207−2.339004 0.293 13 PDE6G 0.200 −2.346579 0.300 13 TULP1 0.192 −2.3517770.308 13 GNGT1 0.156 −2.405413 0.344 13 SAG 0.153 −2.429798 0.347 13 RHO0.157 −2.459338 0.343 13 RPGRIP1 0.224 −2.497198 0.276 13 cluster no. 14DE = 127 CARTPT 0.995 5.703726 0.495 14 TFAP2B 0.971 3.040128 0.471 14GNG2 0.921 2.521110 0.421 14 GAD1 0.935 2.313316 0.435 14 RAB3C 0.9062.257741 0.406 14 6430548M08RIK 0.917 2.251898 0.417 14 MARCKS 0.9492.228788 0.449 14 C1QL1 0.891 2.174893 0.391 14 GPR22 0.860 2.1306020.360 14 PCP4 0.929 2.085684 0.429 14 2610017I09RIK 0.880 2.047078 0.38014 4833424O15RIK 0.884 2.046187 0.384 14 ATP1B1 0.930 2.002380 0.430 14C1QL2 0.851 1.948192 0.351 14 RPH3A 0.886 1.922752 0.386 14 SYT10 0.8261.921924 0.326 14 CAMK4 0.844 1.906300 0.344 14 ISOC1 0.833 1.8368120.333 14 SLC35D3 0.829 1.831320 0.329 14 NR4A2 0.816 1.806155 0.316 14GRIA3 0.827 1.723420 0.327 14 NRXN2 0.841 1.694523 0.341 14 KIT 0.7911.692597 0.291 14 RPRM 0.787 1.685930 0.287 14 CELF4 0.901 1.6841780.401 14 PBX1 0.896 1.668218 0.396 14 SYT7 0.822 1.654737 0.322 14 SYT40.833 1.635617 0.333 14 KCNIP1 0.830 1.617504 0.330 14 FBXW7 0.8411.574306 0.341 14 ITM2C 0.876 1.542051 0.376 14 TENM1 0.766 1.5389490.266 14 NAP1L5 0.860 1.532501 0.360 14 CACNA2D2 0.808 1.530876 0.308 14GNG3 0.851 1.511727 0.351 14 ELAVL4 0.791 1.506871 0.291 14 POU3F3 0.7721.496067 0.272 14 TFAP2A 0.793 1.479966 0.293 14 HOMER2 0.725 1.4534400.225 14 TBX3 0.763 1.424956 0.263 14 CAR8 0.751 1.411188 0.251 14 TSHZ10.787 1.379317 0.287 14 BC048943 0.816 1.375829 0.316 14 SLC32A1 0.7991.373823 0.299 14 CAMKV 0.782 1.366152 0.282 14 PDE3A 0.744 1.3571710.244 14 CNKSR2 0.725 1.353715 0.225 14 SNHG11 0.855 1.350103 0.355 14GABRA2 0.753 1.348395 0.253 14 UCHL1 0.839 1.339151 0.339 14 STMN2 0.8161.321500 0.316 14 AMIGO2 0.761 1.315679 0.261 14 YWHAH 0.814 1.2932290.314 14 MARCKSL1 0.784 1.286051 0.284 14 ANKS1B 0.759 1.281614 0.259 14NDRG4 0.813 1.274413 0.313 14 GAP43 0.749 1.266684 0.249 14 AUTS2 0.7831.256839 0.283 14 SYNPR 0.820 1.249817 0.320 14 ATP2B1 0.869 1.2385710.369 14 GRM1 0.726 1.231165 0.226 14 CPLX3 0.835 1.226050 0.335 14EPB4.1L4A 0.746 1.225236 0.246 14 SOBP 0.717 1.225089 0.217 14 LRRN30.732 1.221377 0.232 14 CYGB 0.762 1.207406 0.262 14 E530001K10RIK 0.7171.204510 0.217 14 COL23A1 0.771 1.203158 0.271 14 VSNL1 0.742 1.1947540.242 14 GM27031 0.701 1.194087 0.201 14 YWHAG 0.788 1.175123 0.288 14A030009H04RIK 0.773 1.169740 0.273 14 PHACTR3 0.756 1.169124 0.256 14RYR2 0.743 1.167697 0.243 14 ZCCHC18 0.790 1.167592 0.290 14 NFIA 0.7201.165989 0.220 14 EFR3A 0.790 1.165206 0.290 14 ELAVL3 0.757 1.1643120.257 14 SH3BGRL 0.726 1.143244 0.226 14 PAX6 0.795 1.121544 0.295 14CTNNA2 0.743 1.115757 0.243 14 VAMP4 0.726 1.103188 0.226 14 SCG2 0.8431.100054 0.343 14 LIN7A 0.801 1.099208 0.301 14 IMPACT 0.745 1.0930910.245 14 NGFRAP1 0.787 1.076352 0.287 14 ARHGAP20 0.706 1.071535 0.20614 PODXL2 0.773 1.071004 0.273 14 ID4 0.704 1.060790 0.204 14 SPOCK30.761 1.053007 0.261 14 BASP1 0.790 1.045714 0.290 14 GRM5 0.7131.040980 0.213 14 DPP6 0.740 1.039731 0.240 14 FAM49A 0.706 1.0372270.206 14 MLLT11 0.749 1.033558 0.249 14 ACOT7 0.736 1.033349 0.236 14RIT2 0.729 1.029466 0.229 14 6330403K07RIK 0.710 1.028243 0.210 14SERPINE2 0.706 1.024427 0.206 14 TMSB10 0.795 1.017801 0.295 14 WDR10.746 1.015410 0.246 14 SNCB 0.802 1.013614 0.302 14 STMN3 0.7511.009106 0.251 14 ZEB2 0.734 1.007237 0.234 14 TTC3 0.821 1.005346 0.32114 TRANK1 0.710 1.001051 0.210 14 HMGN1 0.252 −1.261384 0.248 14 GNB10.278 −1.308646 0.222 14 RP1 0.272 −1.542408 0.228 14 UNC119 0.251−1.556548 0.249 14 RCVRN 0.262 −1.576865 0.238 14 PDE6G 0.243 −1.5957530.257 14 ROM1 0.252 −1.638720 0.248 14 TULP1 0.238 −1.644062 0.262 14CNGA1 0.290 −1.645086 0.210 14 PDC 0.207 −1.653719 0.293 14 GNAT1 0.231−1.672780 0.269 14 PDE6B 0.255 −1.698852 0.245 14 PRPH2 0.219 −1.7006650.281 14 NRL 0.285 −1.702971 0.215 14 GNGT1 0.191 −1.727437 0.309 14NR2E3 0.274 −1.735667 0.226 14 SLC24A1 0.284 −1.736471 0.216 14 SAG0.186 −1.773021 0.314 14 RPGRIP1 0.260 −1.792548 0.240 14 RHO 0.186−1.793033 0.314 14 RS1 0.268 −1.840885 0.232 14 cluster no. 15 DE = 69SLC17A8 1.000 3.971625 0.500 15 LAMP5 0.940 2.673730 0.440 15A930001A20R1K 0.889 2.597410 0.389 15 CAR3 0.835 2.514193 0.335 15TFAP2B 0.905 2.503643 0.405 15 GRIA3 0.826 2.061066 0.326 15 GABRA20.842 2.031614 0.342 15 PCP4 0.909 1.973695 0.409 15 CDC7 0.832 1.9558720.332 15 SNHG11 0.887 1.937983 0.387 15 VSTM2L 0.832 1.918272 0.332 15STMN2 0.849 1.904450 0.349 15 CAMK2N1 0.861 1.838364 0.361 15 THSD7A0.787 1.831897 0.287 15 ITM2B 0.910 1.821993 0.410 15 SPHKAP 0.8311.715234 0.331 15 RBFOX1 0.735 1.705497 0.235 15 OLFM1 0.839 1.6595070.339 15 CACNG4 0.815 1.640851 0.315 15 PDE1C 0.762 1.600665 0.262 15NXPH1 0.756 1.565593 0.256 15 TFAP2A 0.747 1.543928 0.247 15 CELF4 0.8411.542615 0.341 15 CADM3 0.799 1.512073 0.299 15 SLC24A3 0.743 1.5060170.243 15 HPGD 0.706 1.448453 0.206 15 GPHN 0.809 1.446959 0.309 15 GNG30.818 1.418323 0.318 15 NEUROD2 0.737 1.357057 0.237 15 2900011O08R1K0.772 1.324460 0.272 15 NXPH3 0.734 1.317785 0.234 15 MARCKS 0.8151.293783 0.315 15 RAB3C 0.739 1.288257 0.239 15 CDK14 0.739 1.2869330.239 15 SORCS1 0.717 1.234444 0.217 15 CALM1 0.893 1.233054 0.393 15A830010M20RIK 0.747 1.230927 0.247 15 SIX6 0.750 1.213235 0.250 15 NSG20.731 1.208784 0.231 15 SNCB 0.795 1.174871 0.295 15 NREP 0.813 1.1678850.313 15 TAGLN3 0.765 1.156591 0.265 15 NSG1 0.707 1.149341 0.207 15CHGA 0.768 1.148225 0.268 15 MEG3 0.820 1.127476 0.320 15 GRIA2 0.7861.124935 0.286 15 ELAVL3 0.721 1.121228 0.221 15 NNAT 0.713 1.0973240.213 15 CALM2 0.818 1.097061 0.318 15 NRXN2 0.746 1.092058 0.246 15TCEAL5 0.701 1.076692 0.201 15 PGM2L1 0.749 1.071344 0.249 15 RUNX1T10.726 1.057725 0.226 15 RTN1 0.787 1.038594 0.287 15 NRXN3 0.7571.036936 0.257 15 HLF 0.729 1.032907 0.229 15 TTC3 0.783 1.000773 0.28315 A030009H04RIK 0.710 1.000074 0.210 15 GNAT1 0.299 −1.040079 0.201 15GNB1 0.299 −1.128978 0.201 15 PDE6G 0.299 −1.189289 0.201 15 PRPH2 0.281−1.204277 0.219 15 TULP1 0.275 −1.241916 0.225 15 SAG 0.232 −1.2598840.268 15 ROM1 0.278 −1.321566 0.222 15 RCVRN 0.291 −1.325043 0.209 15PDC 0.246 −1.329612 0.254 15 GNGT1 0.240 −1.347078 0.260 15 RHO 0.227−1.442002 0.273 15 cluster no. 16 DE = 97 LAMP5 0.946 2.657760 0.446 16GJD2 0.928 2.371019 0.428 16 DNER 0.912 2.349418 0.412 16 TFAP2B 0.9372.307419 0.437 16 SLC6A9 0.877 2.261401 0.377 16 DYNC1I1 0.871 2.2388460.371 16 CAR2 0.951 2.212296 0.451 16 TMEM132A 0.830 2.024931 0.330 16HSPA12A 0.882 2.015750 0.382 16 EIF1B 0.886 2.008369 0.386 16 NCALD0.858 1.949536 0.358 16 RNF152 0.834 1.859704 0.334 16 CALM1 0.9491.848818 0.449 16 CPLX3 0.910 1.811801 0.410 16 GRIA3 0.813 1.8037830.313 16 CALB1 0.817 1.799962 0.317 16 ATP1B1 0.887 1.769979 0.387 16NDRG4 0.841 1.747721 0.341 16 CAMKV 0.808 1.717383 0.308 16 CCSAP 0.7611.662431 0.261 16 PTPRF 0.775 1.659107 0.275 16 RCAN2 0.772 1.6428530.272 16 STAC2 0.756 1.591278 0.256 16 DLGAP1 0.780 1.588752 0.280 16DAB1 0.780 1.587313 0.280 16 SCN1A 0.754 1.580647 0.254 16 SLC24A2 0.7281.578024 0.228 16 ZYX 0.743 1.492083 0.243 16 NFIA 0.764 1.487009 0.26416 PROX1 0.827 1.483800 0.327 16 PLCH1 0.751 1.482505 0.251 16 FGF10.739 1.462304 0.239 16 ELAVL3 0.781 1.425611 0.281 16 ZFP804A 0.7271.413891 0.227 16 FSTL5 0.765 1.396307 0.265 16 PHLDA1 0.707 1.3891060.207 16 PPP1R1A 0.773 1.373425 0.273 16 6430548M08RIK 0.808 1.3712000.308 16 LSAMP 0.751 1.359807 0.251 16 SPOCK3 0.746 1.352438 0.246 16KCNMA1 0.784 1.346329 0.284 16 PAK7 0.751 1.343190 0.251 16 ATP6V1G20.757 1.336798 0.257 16 KIF5C 0.756 1.296446 0.256 16 TSPAN7 0.8541.277924 0.354 16 FBXW7 0.753 1.273232 0.253 16 SYNPR 0.759 1.2634140.259 16 CACNG3 0.704 1.254853 0.204 16 DARC 0.722 1.251447 0.222 16OSBPL1A 0.724 1.244547 0.224 16 MEG3 0.832 1.232034 0.332 16 SV2A 0.8101.225364 0.310 16 A030009H04RIK 0.718 1.223471 0.218 16 TAGLN3 0.7641.222365 0.264 16 ANKS1B 0.716 1.213048 0.216 16 GRIA4 0.728 1.1655640.228 16 SLC32A1 0.719 1.163084 0.219 16 QDPR 0.713 1.151071 0.213 16TCEAL5 0.724 1.146794 0.224 16 RIT2 0.742 1.138978 0.242 16 TPI1 0.7901.128863 0.290 16 DPP6 0.712 1.125116 0.212 16 BNIP3 0.705 1.1161620.205 16 PODXL2 0.750 1.108498 0.250 16 ZEB2 0.706 1.105841 0.206 16RAB3C 0.706 1.104219 0.206 16 TUBB2A 0.758 1.097099 0.258 16 PHYHIPL0.721 1.053411 0.221 16 NSG2 0.707 1.039994 0.207 16 CADM3 0.7241.033579 0.224 16 PNMAL2 0.726 1.032390 0.226 16 ITM2C 0.757 1.0317380.257 16 GRIA2 0.742 1.020469 0.242 16 NRXN3 0.740 1.019019 0.240 16SPHKAP 0.713 1.014996 0.213 16 ANK3 0.715 1.004342 0.215 16 HMGN1 0.215−1.521153 0.285 16 GNB1 0.229 −1.683458 0.271 16 CNGA1 0.271 −1.7080740.229 16 UNC119 0.244 −1.715525 0.256 16 RPGRIP1 0.264 −1.737171 0.23616 ROM1 0.234 −1.740653 0.266 16 NRL 0.265 −1.762281 0.235 16 RS1 0.265−1.774883 0.235 16 PDE6B 0.237 −1.791541 0.263 16 RP1 0.240 −1.8185560.260 16 PRPH2 0.201 −1.822970 0.299 16 RCVRN 0.225 −1.829448 0.275 16PDE6G 0.212 −1.836061 0.288 16 GNGT1 0.177 −1.911169 0.323 16 NR2E30.252 −1.935120 0.248 16 SLC24A1 0.268 −1.939047 0.232 16 TULP1 0.202−1.958300 0.298 16 PDC 0.178 −1.988325 0.322 16 GNAT1 0.203 −2.0054050.297 16 RHO 0.170 −2.014559 0.330 16 SAG 0.157 −2.131605 0.343 16cluster no. 17 DE = 99 NHLH2 0.955 2.801308 0.455 17 PTPRF 0.9382.711222 0.438 17 IGF1 0.893 2.396873 0.393 17 SLC6A9 0.922 2.3917290.422 17 LAMP5 0.894 2.317776 0.394 17 NECAB1 0.845 2.034798 0.345 17NFIX 0.842 2.031417 0.342 17 QDPR 0.864 2.017375 0.364 17 RPH3A 0.8611.948967 0.361 17 TFAP2C 0.804 1.906681 0.304 17 EBF3 0.816 1.8976810.316 17 ZFP804A 0.806 1.817066 0.306 17 CPLX3 0.918 1.803041 0.418 17CRABP1 0.796 1.772659 0.296 17 NR2F2 0.779 1.746596 0.279 17 HPCA 0.8041.734854 0.304 17 ELAVL3 0.846 1.731296 0.346 17 NRSN1 0.810 1.6748210.310 17 IER5 0.778 1.651591 0.278 17 PTPRT 0.756 1.624019 0.256 17 DAB10.802 1.623759 0.302 17 TUBB2A 0.848 1.623271 0.348 17 LGR5 0.7571.617618 0.257 17 NCALD 0.795 1.603750 0.295 17 VSTM2A 0.740 1.5547220.240 17 CELF4 0.872 1.530692 0.372 17 SULF2 0.760 1.520666 0.260 17MGLL 0.754 1.520539 0.254 17 PAX6 0.816 1.498468 0.316 17 SLC24A3 0.7811.478973 0.281 17 PAM 0.742 1.475693 0.242 17 CABP1 0.775 1.471362 0.27517 CACNG3 0.735 1.458559 0.235 17 SLC32A1 0.764 1.449804 0.264 17 HS6ST20.707 1.397958 0.207 17 THRA 0.819 1.389414 0.319 17 NAV1 0.774 1.3795210.274 17 SPARCL1 0.752 1.366591 0.252 17 DPP6 0.726 1.359750 0.226 17TCF4 0.820 1.358693 0.320 17 NECAB2 0.717 1.353128 0.217 17 APP 0.8281.351232 0.328 17 LY6H 0.730 1.336108 0.230 17 TTC3 0.870 1.328177 0.37017 SYT4 0.748 1.315258 0.248 17 EBF1 0.701 1.310439 0.201 17 CALB2 0.8021.299700 0.302 17 TKT 0.761 1.294344 0.261 17 CAMKV 0.709 1.291859 0.20917 SPHKAP 0.771 1.288256 0.271 17 FSTL5 0.725 1.283969 0.225 17 THY10.723 1.277498 0.223 17 SUSD4 0.709 1.255558 0.209 17 GRIA4 0.7351.236041 0.235 17 4930447C04RIK 0.756 1.222306 0.256 17 SEZ6 0.7131.213564 0.213 17 FILIP1L 0.701 1.211433 0.201 17 MARCKSL1 0.7441.207456 0.244 17 ANK3 0.761 1.200975 0.261 17 NRXN3 0.807 1.1687880.307 17 NDUFC2 0.787 1.159975 0.287 17 GPM6A 0.780 1.143074 0.280 17ITM2C 0.768 1.128670 0.268 17 SV2A 0.779 1.093330 0.279 17 SNHG11 0.8251.085316 0.325 17 LSAMP 0.709 1.058888 0.209 17 GAS6 0.767 1.0585200.267 17 CAMK2N1 0.762 1.055403 0.262 17 SCG3 0.751 1.049366 0.251 17NSG2 0.706 1.049170 0.206 17 CRMP1 0.709 1.036034 0.209 17 MEG3 0.8391.025407 0.339 17 NREP 0.775 1.017209 0.275 17 PGRMC1 0.723 1.0139920.223 17 PPP1R1A 0.707 1.008115 0.207 17 INA 0.720 1.004427 0.220 17HMGN1 0.257 −1.196552 0.243 17 CST3 0.297 −1.331354 0.203 17 GNB1 0.257−1.407515 0.243 17 CNGA1 0.284 −1.538745 0.216 17 UNC119 0.258 −1.5669380.242 17 NEUROD1 0.288 −1.572623 0.212 17 ROM1 0.243 −1.577979 0.257 17NRL 0.281 −1.587397 0.219 17 PRPH2 0.211 −1.721597 0.289 17 SLC24A10.279 −1.725891 0.221 17 TULP1 0.219 −1.731480 0.281 17 RP1 0.244−1.732042 0.256 17 NR2E3 0.264 −1.737427 0.236 17 RS1 0.266 −1.7475430.234 17 RCVRN 0.233 −1.757940 0.267 17 RPGRIP1 0.258 −1.766938 0.242 17PDE6G 0.220 −1.771881 0.280 17 PDE6B 0.236 −1.776243 0.264 17 GNAT10.216 −1.796601 0.284 17 PDC 0.191 −1.801008 0.309 17 RHO 0.181−1.842355 0.319 17 SAG 0.174 −1.848204 0.326 17 GNGT1 0.181 −1.8781520.319 17 cluster no. 18 DE = 76 myA UC myDiff po wer cl ust NHLH2 0.9 402 .577919 440 18 0. PCDH17 0.9 26 2 .518747 426 18 0. NFIX 0.8 96 2.289617 396 18 0. HPCA 0.8 94 2 .165617 394 18 0. NFIB 0.8 50 2 .151836350 18 0. CHN2 0.8 65 1 .981338 365 18 0. NECAB1 0.8 34 1 .930261 334 180. CELF4 0.9 44 1 .891838 444 18 0. COL12A1 0.7 69 1 .884139 269 18 0.PRDM13 0.7 95 1 .854160 295 18 0. D3BWG0562E 30 1 .829089 330 18 D3 0.80. TCF4 0.8 92 1 .827289 392 18 0. NRXN1 0.7 67 1 .826387 267 18 0.SOCS2 0.7 95 1 .761385 295 18 0. ANK3 0.8 44 1 .673902 344 18 0. TFAP2C0.7 59 1 .629828 259 18 0. STMN2 0.7 49 1 .556131 249 18 0. ZFP804A 0.719 1 .551147 219 18 0. APP 0.8 75 1 .546885 375 18 0. ELAVL3 0.7 83 1.506019 283 18 0. ARHGAP20 0.7 19 1 .505211 219 18 0. MEG3 0.8 80 1.462490 380 18 0. SLC32A1 0.7 65 1 .444429 265 18 0. NAV1 0.7 62 1.417519 262 18 0. SEMA4G 0.7 29 1 .383182 229 18 0. MARCKSL1 0.7 76 1.359972 276 18 0. PIK3R3 0.7 45 1 .354144 245 18 0. THRA 0.8 20 1.353685 320 18 0. NCALD 0.7 36 1 .337872 236 18 0. NSG1 0.7 42 1 .320977242 18 0. PTPRS 0.7 43 1 .286383 243 18 0. NREP 0.8 40 1 .285992 340 180. CABP1 0.7 25 1 .262818 225 18 0. SIX3 0.7 87 1 .251619 287 18 0.SLC6A9 0.7 10 1 .245464 210 18 0. RPH3A 0.7 52 1 .238243 252 18 0. TTC30.8 42 1 .233544 342 18 0. GRIA2 0.7 77 1 .228039 277 18 0. CD47 0.7 531 .210868 253 18 0. ATP1B1 0.8 01 1 .167177 301 18 0. ZCCHC18 0.7 20 1.164194 220 18 0. PLEKHA1 0.7 52 1 .163094 252 18 0. GPM6A 0.7 88 1.153552 288 18 0. PNMAL2 0.7 48 1 .130451 248 18 0. GRIA4 0.7 25 1.120343 225 18 0. RTN1 0.7 73 1 .099410 273 18 0. TUBB2A 0.7 69 1.094495 269 18 0. CAMK2N1 0.7 42 1 .088043 242 18 0. CALM2 0.7 98 1.074762 298 18 0. TAGLN3 0.7 19 1 .054396 219 18 0. NRXN3 0.7 54 1.040204 254 18 0. PAX6 0.7 34 1 .034451 234 18 0. NGFRAP1 0.7 39 1.019194 239 18 0. HMGN1 0.2 51 −1 .229929 249 18 0. CST3 0.2 91 −1.416269 209 18 0. GNB1 0.2 47 −1 .445738 253 18 0. RPGRIP1 0.2 83 −1.546356 217 18 0. NRL 0.2 89 −1 .564782 211 18 0. NEUROD1 0.2 83 −1.620185 217 18 0. NR2E3 0.2 75 −1 .669162 225 18 0. PDE6B 0.2 54 −1.672037 246 18 0. UNC119 0.2 44 −1 .678390 256 18 0. RP1 0.2 48 −1.709894 252 18 0. SLC24A1 0.2 87 −1 .717416 213 18 0. PDC 0.1 98 −1.748702 302 18 0. ROM1 0.2 30 −1 .751335 270 18 0. TULP1 0.2 18 −1.761842 282 18 0. PDE6G 0.2 26 −1 .763229 274 18 0. RCVRN 0.2 31 −1.769978 269 18 0. SAG 0.1 84 −1 .774554 316 18 0. CNGA1 0.2 65 −1.786474 235 18 0. GNGT1 0.1 89 −1 .797833 311 18 0. RS1 0.2 68 −1.853854 232 18 0. GNAT1 0.2 14 −1 .946696 286 18 0. PRPH2 0.2 02 −1.956290 298 18 0. RHO 0.1 80 −2 .007748 320 18 0. cluster no. 19 DE =115 myAUC myDiff power cluster # LAMP5 0.966 2.812286 0.466 19 GABRA10.897 2.484680 0.397 19 SLC24A3 0.927 2.393144 0.427 19 NHLH2 0.9452.383320 0.445 19 LY6H 0.876 2.116752 0.376 19 EBF1 0.874 2.024209 0.37419 SNHG11 0.922 1.988360 0.422 19 NDRG4 0.876 1.960583 0.376 19 CDH220.815 1.785911 0.315 19 SPHKAP 0.886 1.743169 0.386 19 PNMAL2 0.8671.735673 0.367 19 SIX3 0.851 1.695121 0.351 19 PTPRT 0.803 1.6876760.303 19 PTGDS 0.783 1.682383 0.283 19 SLC6A9 0.811 1.678064 0.311 19CAMKV 0.818 1.675469 0.318 19 NRXN2 0.848 1.674929 0.348 19 ELAVL3 0.8621.653420 0.362 19 PTPRD 0.849 1.648261 0.349 19 SYT13 0.813 1.6258620.313 19 CHN2 0.797 1.618956 0.297 19 AQP6 0.736 1.613186 0.236 19 CABP10.840 1.607853 0.340 19 TCF4 0.879 1.577171 0.379 19 LDHB 0.829 1.5659480.329 19 RAB3C 0.777 1.545867 0.277 19 PRDM13 0.768 1.521082 0.268 19INA 0.852 1.511391 0.352 19 SIX6 0.783 1.490271 0.283 19 KCTD8 0.7661.472089 0.266 19 MEG3 0.905 1.468522 0.405 19 PAX6 0.823 1.451718 0.32319 APP 0.852 1.450537 0.352 19 OGFRL1 0.821 1.437451 0.321 19 ATP1B10.855 1.426796 0.355 19 6430548M08RIK 0.803 1.419158 0.303 19 NECAB10.749 1.374682 0.249 19 VAT1L 0.743 1.371743 0.243 19 NNAT 0.7221.357449 0.222 19 NRSN1 0.790 1.356337 0.290 19 DPP6 0.765 1.3554990.265 19 NSG1 0.771 1.344649 0.271 19 TKT 0.806 1.341063 0.306 19 CDK140.761 1.337859 0.261 19 FRRS1L 0.709 1.335420 0.209 19 OSBPL1A 0.7521.329635 0.252 19 MGLL 0.763 1.294623 0.263 19 GABRG2 0.757 1.2913740.257 19 GNG3 0.828 1.268832 0.328 19 GRIA2 0.830 1.263501 0.330 19BASP1 0.810 1.253882 0.310 19 STMN3 0.809 1.238855 0.309 19 GAS7 0.7111.233308 0.211 19 CELF4 0.831 1.232486 0.331 19 SPOCK3 0.771 1.2313140.271 19 DLG2 0.718 1.209247 0.218 19 STMN4 0.732 1.207910 0.232 19ZFP804A 0.711 1.206180 0.211 19 SPARCL1 0.760 1.196819 0.260 19 THRA0.783 1.194146 0.283 19 MLLT11 0.751 1.190315 0.251 19 GRIA3 0.7221.173347 0.222 19 TCEAL5 0.740 1.171672 0.240 19 GABRB2 0.707 1.1671030.207 19 LHFP 0.721 1.165278 0.221 19 HMGCS1 0.731 1.155608 0.231 19UBASH3B 0.710 1.154651 0.210 19 TMEM215 0.764 1.134491 0.264 19 TAGLN30.797 1.134360 0.297 19 HSD17B12 0.778 1.130471 0.278 19 SLC32A1 0.7331.119009 0.233 19 ABAT 0.708 1.118345 0.208 19 CALM2 0.829 1.1051430.329 19 ATPIF1 0.795 1.102584 0.295 19 GNAS 0.833 1.076868 0.333 19SYT4 0.779 1.071587 0.279 19 TTC3 0.832 1.066694 0.332 19 CAMK2N1 0.7681.054984 0.268 19 TUBB2A 0.780 1.041674 0.280 19 RIT2 0.712 1.0395860.212 19 PIK3R3 0.717 1.034720 0.217 19 SV2A 0.772 1.033485 0.272 19CAMK2A 0.701 1.028493 0.201 19 NGFRAP1 0.770 1.026982 0.270 19A030009H04RIK 0.719 1.026299 0.219 19 GPM6A 0.792 1.021982 0.292 19NAP1L5 0.759 1.016867 0.259 19 MAPT 0.724 1.007727 0.224 19 NDN 0.7171.007103 0.217 19 ATP6V1G2 0.711 1.000069 0.211 19 CST3 0.295 −1.4646540.205 19 GNB1 0.232 −1.731344 0.268 19 HMGN1 0.193 −1.764691 0.307 19FAM57B 0.287 −1.846219 0.213 19 UNC119 0.235 −1.869744 0.265 19 AIPL10.299 −1.912009 0.201 19 NEUROD1 0.267 −1.949197 0.233 19 CNGA1 0.258−2.018138 0.242 19 ROM1 0.220 −2.018487 0.280 19 RP1 0.224 −2.0251880.276 19 NR2E3 0.250 −2.051380 0.250 19 PDE6B 0.216 −2.080446 0.284 19RS1 0.250 −2.098084 0.250 19 PRPH2 0.185 −2.112352 0.315 19 RCVRN 0.209−2.119590 0.291 19 SLC24A1 0.260 −2.160451 0.240 19 NRL 0.243 −2.1716000.257 19 PDE6G 0.194 −2.189464 0.306 19 TULP1 0.190 −2.209461 0.310 19GNAT1 0.190 −2.263062 0.310 19 SAG 0.144 −2.317843 0.356 19 GNGT1 0.153−2.323731 0.347 19 RHO 0.162 −2.332956 0.338 19 RPGRIP1 0.228 −2.4017600.272 19 PDC 0.156 −2.470951 0.344 19 Diff myAUC my power cluster # gecluster no. 20 DE = 43 PPP1R17 0.909 3.02 8071 20 PPP1R 0.409 EBF3 0.7912.15 8191 20 EB 0.291 LGR5 0.772 2.11 3992 20 LG 0.272 EBF1 0.743 1.978420 20 EB 0.243 IGFBP5 0.726 1.93 2417 20 IGFB 0.226 TCF4 0.834 1.740057 20 TC 0.334 PNMAL2 0.785 1.72 2746 20 PNMA 0.285 ZFP804A 0.714 1.712913 20 ZFP80 0.214 ELAVL3 0.751 1.65 7175 20 ELAV 0.251 SNCA 0.723 1.631290 20 SN 0.223 LY6H 0.712 1.60 0690 20 LY 0.212 INA 0.743 1.58 6423 20I 0.243 CACNG4 0.702 1.42 8349 20 CACN 0.202 MARCKS 0.777 1.38 4398 20MARC 0.277 GRIA2 0.746 1.29 4026 20 GRI 0.246 SPHKAP 0.722 1.28 5598 20SPHK 0.222 CALB2 0.719 1.27 4202 20 CAL 0.219 MEG3 0.813 1.26 2649 20 ME0.313 BASP1 0.724 1.23 1810 20 BAS 0.224 RTN1 0.750 1.22 6570 20 RT0.250 CELF4 0.769 1.22 0263 20 CEL 0.269 NEUROD4 0.719 1.14 3353 20NEURO 0.219 GNG3 0.711 1.10 4068 20 GN 0.211 SYT1 0.807 1.04 4134 20 SY0.307 TTC3 0.768 1.02 9450 20 TT 0.268 HMGN1 0.273 −1.01 4397 20 HMG0.227 GNB1 0.284 −1.07 5547 20 GN 0.216 ROM1 0.274 −1.14 4841 20 RO0.226 UNC119 0.276 −1.17 8787 20 UNC1 0.224 GNAT1 0.261 −1.19 3799 20GNA 0.239 GNGT1 0.225 −1.28 0242 20 GNG 0.275 PDE6G 0.253 −1.28 9229 20PDE 0.247 PRPH2 0.237 −1.30 6099 20 PRP 0.263 RP1 0.270 −1.31 2369 20 R0.230 RHO 0.219 −1.31 4846 20 R 0.281 RCVRN 0.254 −1.31 7434 20 RCV0.246 RS1 0.290 −1.31 7916 20 R 0.210 PDC 0.224 −1.32 7322 20 P 0.276TULP1 0.243 −1.33 8314 20 TUL 0.257 PDE6B 0.266 −1.34 2076 20 PDE 0.234CNGA1 0.283 −1.37 9756 20 CNG 0.217 RPGRIP1 0.282 −1.42 3791 20 RPGRI0.218 SAG 0.196 −1.47 6851 20 S 0.304 cluster no. 21 DE = 45 NHLH2 0.9433.05 4281 21 NHL 0.443 NFIX 0.847 2.29 9079 21 NF 0.347 CRABP1 0.8422.27 6418 21 CRAB 0.342 CCK 0.742 2.07 4822 21 C 0.242 GRIK2 0.782 2.070961 21 GRI 0.282 HPCA 0.803 2.00 5328 21 HP 0.303 ELAVL3 0.824 1.888644 21 ELAV 0.324 PRKCB 0.802 1.86 1453 21 PRK 0.302 CNTN6 0.738 1.836086 21 CNT 0.238 NCKAP5 0.741 1.83 1134 21 NCKA 0.241 LGR5 0.714 1.748355 21 LG 0.214 EBF1 0.734 1.71 4978 21 EB 0.234 NRXN1 0.724 1.69 338521 NRX 0.224 CELF4 0.853 1.68 7320 21 CEL 0.353 TCF4 0.839 1.67 9788 21TC 0.339 PRDM13 0.709 1.67 9478 21 PRDM 0.209 CHN2 0.721 1.62 1249 21 CH0.221 GNAL 0.708 1.58 7639 21 GN 0.208 KCND3 0.701 1.57 6876 21 KCN0.201 ZFP804A 0.710 1.56 4564 21 ZFP80 0.210 SLC24A3 0.751 1.54 4541 21SLC24 0.251 APC 0.810 1.49 8604 21 A 0.310 ANK3 0.775 1.40 2792 21 AN0.275 CAMK2N1 0.768 1.37 7643 21 CAMK2 0.268 PNMAL2 0.740 1.36 3728 21PNMA 0.240 GRIA2 0.765 1.32 0910 21 GRI 0.265 SPHKAP 0.749 1.30 6807 21SPHK 0.249 CALM2 0.811 1.26 1951 21 CAL 0.311 MEG3 0.844 1.24 7565 21 ME0.344 APP 0.745 1.13 2361 21 A 0.245 TTC3 0.794 1.11 6633 21 TT 0.294GPM6A 0.706 1.10 4331 21 GPM 0.206 UNC119 0.296 −1.16 3773 21 UNC1 0.204RP1 0.295 −1.18 0835 21 R 0.205 ROM1 0.285 −1.18 8372 21 RO 0.215 PDE6G0.275 −1.19 3017 21 PDE 0.225 PDE6B 0.286 −1.24 4644 21 PDE 0.214 TULP10.264 −1.25 7146 21 TUL 0.236 RHO 0.234 −1.26 0099 21 R 0.266 RCVRN0.272 −1.27 2038 21 RCV 0.228 SAG 0.226 −1.28 7003 21 S 0.274 PRPH20.250 −1.29 1410 21 PRP 0.250 PDC 0.235 −1.29 4464 21 P 0.265 GNGT10.234 −1.29 5401 21 GNG 0.266 GNAT1 0.262 −1.29 9206 21 GNA 0.238 myAUCmyDiff power cluster # cluster no. 22 DE = 51 LAMP5 0.944 2.824713 0.44422 TFAP2B 0.872 2.223340 0.372 22 CACNG4 0.834 1.969710 0.334 22 ZFP804A0.751 1.834667 0.251 22 DPP6 0.764 1.729152 0.264 22 GRIA1 0.7181.703132 0.218 22 NEUROD2 0.712 1.641371 0.212 22 CELF4 0.860 1.6224710.360 22 PAX6 0.803 1.597197 0.303 22 SLC6A9 0.760 1.571800 0.260 22MEG3 0.866 1.469502 0.366 22 2900011O08RIK 0.729 1.446080 0.229 22ELAVL3 0.749 1.390450 0.249 22 RAB3C 0.713 1.382919 0.213 22 NRSN1 0.7021.336043 0.202 22 PNMAL2 0.747 1.334122 0.247 22 TCF4 0.788 1.3297260.288 22 GRIA2 0.780 1.313318 0.280 22 MARCKSL1 0.716 1.298641 0.216 22SLC32A1 0.704 1.296328 0.204 22 SNHG11 0.784 1.279440 0.284 22 MAPT0.702 1.244966 0.202 22 NRXN2 0.701 1.211145 0.201 22 GNG3 0.7601.195139 0.260 22 NAP1L5 0.724 1.176074 0.224 22 TTC3 0.805 1.1718540.305 22 TAGLN3 0.710 1.156623 0.210 22 PTPRD 0.717 1.099502 0.217 22BASP1 0.727 1.088889 0.227 22 THRA 0.713 1.076652 0.213 22 SV2A 0.7471.060584 0.247 22 SNCB 0.757 1.048856 0.257 22 PLEKHA1 0.702 1.0252310.202 22 GPM6A 0.708 1.019030 0.208 22 HMGN1 0.273 −1.040507 0.227 22GNB1 0.285 −1.170599 0.215 22 PDE6B 0.293 −1.193748 0.207 22 RP1 0.295−1.213102 0.205 22 UNC119 0.278 −1.263254 0.222 22 PRPH2 0.245 −1.3158240.255 22 PDE6G 0.264 −1.337712 0.236 22 RPGRIP1 0.288 −1.352712 0.212 22PDC 0.226 −1.365109 0.274 22 TULP1 0.248 −1.369050 0.252 22 GNAT1 0.254−1.389822 0.246 22 NR2E3 0.292 −1.390392 0.208 22 ROM1 0.261 −1.4280900.239 22 GNGT1 0.219 −1.443382 0.281 22 RCVRN 0.259 −1.447967 0.241 22SAG 0.208 −1.466971 0.292 22 RHO 0.216 −1.494424 0.284 22 cluster no. 23DE = 67 TFAP2B 0.928 2.494440 0.428 23 GAD1 0.917 2.437951 0.417 23FBXW7 0.917 2.420581 0.417 23 2610017I09RIK 0.846 2.309127 0.346 23 PCP40.938 2.265534 0.438 23 SLC6A1 0.885 2.235858 0.385 23 DKK3 0.9392.182791 0.439 23 CELF4 0.935 2.157447 0.435 23 GUCY1A3 0.889 2.1080610.389 23 SIX3 0.889 2.095564 0.389 23 C1QL2 0.822 2.067956 0.322 23GUCY1B3 0.865 2.029309 0.365 23 CBFA2T3 0.786 2.026242 0.286 23 POU3F30.772 1.859852 0.272 23 NAP1L5 0.860 1.807160 0.360 23 TKT 0.8361.783663 0.336 23 HPGD 0.751 1.778162 0.251 23 SNHG11 0.895 1.7769250.395 23 ADARB1 0.803 1.745295 0.303 23 GAD2 0.747 1.658875 0.247 23LRRN3 0.768 1.658143 0.268 23 CACNG4 0.822 1.640376 0.322 23 OLFM1 0.7741.633329 0.274 23 MEG3 0.894 1.607437 0.394 23 ELAVL4 0.717 1.4695080.217 23 KCNIP1 0.731 1.459041 0.231 23 KCND3 0.724 1.426750 0.224 23ELAVL3 0.756 1.383776 0.256 23 SLC32A1 0.738 1.352046 0.238 23 GNG30.797 1.337489 0.297 23 NDRG4 0.760 1.318015 0.260 23 HAP1 0.7351.314020 0.235 23 FRMD5 0.721 1.311942 0.221 23 APC 0.800 1.285337 0.30023 TMX4 0.759 1.279036 0.259 23 SCG2 0.808 1.243538 0.308 23 GRIA2 0.7741.215973 0.274 23 LDHB 0.727 1.201661 0.227 23 TTC3 0.838 1.197850 0.33823 BASP1 0.772 1.194948 0.272 23 MARCKSL1 0.704 1.159591 0.204 23GPRASP1 0.738 1.153237 0.238 23 PAX6 0.748 1.152232 0.248 23 HSD17B120.736 1.142303 0.236 23 SIX3OS1 0.721 1.135949 0.221 23 IMPACT 0.7041.129338 0.204 23 6430548M08RIK 0.708 1.125889 0.208 23 TRIM9 0.7111.124665 0.211 23 TAGLN3 0.728 1.095091 0.228 23 SNCB 0.779 1.0678690.279 23 HMGN1 0.286 −1.009380 0.214 23 GNB1 0.270 −1.275684 0.230 23UNC119 0.280 −1.310248 0.220 23 ROM1 0.271 −1.317239 0.229 23 RPGRIP10.295 −1.333701 0.205 23 TULP1 0.243 −1.374221 0.257 23 PDE6G 0.255−1.375311 0.245 23 RCVRN 0.266 −1.381017 0.234 23 PRPH2 0.236 −1.3874000.264 23 PDE6B 0.278 −1.393976 0.222 23 RP1 0.274 −1.402082 0.226 23 RS10.293 −1.450358 0.207 23 GNGT1 0.219 −1.451672 0.281 23 RHO 0.212−1.459768 0.288 23 SAG 0.209 −1.461985 0.291 23 PDC 0.215 −1.4921150.285 23 GNAT1 0.243 −1.525967 0.257 23 cluster no. 24 DE = 49 yDiffmyAUC m powe r clus t RHO 0.945 1.8 57266 5 2 4 0.44 GNAT1 0.889 1.780155 9 2 4 G 0.38 SLC24A1 0.802 1.7 43717 2 2 4 SLC 0.30 PDE6B 0.8551.7 43134 5 2 4 P 0.35 PDC 0.919 1.7 00660 9 2 4 0.41 CNGA1 0.812 1.680377 2 2 4 C 0.31 RP1 0.840 1.6 73527 0 2 4 0.34 SAG 0.930 1.6 50156 02 4 0.43 NR2E3 0.810 1.6 44369 0 2 4 N 0.31 NRL 0.808 1.6 44321 8 2 40.30 GNB1 0.867 1.6 19807 7 2 4 0.36 GNGT1 0.902 1.6 08430 2 2 4 G 0.40PRPH2 0.880 1.5 97904 0 2 4 P 0.38 PDE6A 0.737 1.5 88021 7 2 4 P 0.23PDE6G 0.856 1.5 58813 6 2 4 P 0.35 RCVRN 0.842 1.5 36418 2 2 4 R 0.34RPGRIP1 0.794 1.5 33882 4 2 4 RPG 0.29 RS1 0.790 1.5 19606 0 2 4 0.29GUCA1B 0.707 1.5 06131 7 2 4 GU 0.20 CNGB1 0.715 1.4 95706 5 2 4 C 0.21ROM1 0.820 1.4 77666 0 2 4 0.32 RDH12 0.704 1.4 27972 4 2 4 R 0.20FAM57B 0.731 1.3 66885 1 2 4 FA 0.23 TULP1 0.835 1.3 49889 5 2 4 T 0.33AIPL1 0.706 1.1 64169 6 2 4 A 0.20 HMGN1 0.797 1.1 36452 7 2 4 H 0.29UNC119 0.732 1.0 69530 2 2 4 UN 0.23 SERINC1 0.281 −1.0 08401 9 2 4 SER0.21 BEX2 0.291 −1.0 15902 9 2 4 0.20 ITM2B 0.266 −1.0 43926 4 2 4 I0.23 YWHAB 0.253 −1.0 51200 7 2 4 Y 0.24 MAP4 0.290 −1.0 88812 0 2 40.21 HSP90AB1 0.209 −1.1 88043 1 2 4 HSP9 0.29 GNAS 0.229 −1.2 07829 1 24 0.27 TMSB10 0.290 −1.3 40497 0 2 4 TM 0.21 HMGN3 0.283 −1.3 53477 7 24 H 0.21 SCG3 0.286 −1.3 66486 4 2 4 0.21 CPLX3 0.261 −1.4 40524 9 2 4 C0.23 TTC3 0.215 −1.4 59532 5 2 4 0.28 CELF4 0.277 −1.4 77617 3 2 4 C0.22 ITM2C 0.274 −1.5 36542 6 2 4 I 0.22 GPM6A 0.282 −1.6 04191 8 2 4 G0.21 PTPRD 0.290 −1.6 22257 0 2 4 P 0.21 APP 0.289 −1.6 28911 1 2 4 0.21NRXN3 0.262 −1.6 82084 8 2 4 N 0.23 NME1 0.253 −1.6 87771 7 2 4 0.24GNAO1 0.225 −1.9 02619 5 2 4 G 0.27 CALM1 0.173 −1.9 04185 7 2 4 C 0.32MEG3 0.178 −2.1 49534 2 2 4 0.32 myAUC myDiff power cluster # clusterno. 25 DE = 14 PDE6H 0.981 3.791576 0.481 25 OPN1SW 0.832 3.587490 0.33225 GNGT2 0.964 3.261674 0.464 25 OPN1MW 0.891 3.211129 0.391 25 ARR30.918 3.071492 0.418 25 GNAT2 0.941 3.020245 0.441 25 PDE6C 0.8792.613656 0.379 25 KCNE2 0.853 2.337871 0.353 25 GUCA1A 0.881 1.7902970.381 25 CD59A 0.725 1.742573 0.225 25 CCDC136 0.730 1.673432 0.230 25GNB3 0.831 1.569696 0.331 25 SCG3 0.756 1.297292 0.256 25 4930447C04RIK0.703 1.275268 0.203 25 cluster no. 26 DE = 87 PCP2 0.988 3.533209 0.48826 TRPM1 0.990 3.445746 0.490 26 GNG13 0.968 2.839805 0.468 26 ISL10.948 2.719519 0.448 26 CAR8 0.913 2.699407 0.413 26 PRKCA 0.9372.609664 0.437 26 GPR179 0.900 2.431366 0.400 26 CALM1 0.988 2.4213220.488 26 QPCT 0.875 2.374165 0.375 26 VSX2 0.895 2.348176 0.395 26 PCP40.945 2.313286 0.445 26 GRM6 0.873 2.232811 0.373 26 GNAO1 0.9482.215946 0.448 26 LRTM1 0.886 2.179512 0.386 26 TRNP1 0.855 2.1593610.355 26 CACNA2D3 0.803 2.101927 0.303 26 NME1 0.917 2.066828 0.417 26GM4792 0.870 2.059987 0.370 26 LIN7A 0.875 2.018521 0.375 26 PROX1 0.8502.002116 0.350 26 ABLIM1 0.874 1.975136 0.374 26 CABP5 0.840 1.9346300.340 26 VSTM2B 0.782 1.934535 0.282 26 STRIP2 0.761 1.913167 0.261 26SEBOX 0.763 1.858373 0.263 26 RPA1 0.790 1.856293 0.290 26 CCDC136 0.8031.850276 0.303 26 CHGB 0.903 1.837030 0.403 26 B3GALT2 0.775 1.7441620.275 26 MAP4 0.873 1.732032 0.373 26 RNF152 0.743 1.723092 0.243 26ZBTB20 0.807 1.707863 0.307 26 CNTN4 0.737 1.705791 0.237 26 IFT20 0.8041.668409 0.304 26 CASP7 0.725 1.663103 0.225 26 TMSB10 0.844 1.6595610.344 26 ITM2C 0.829 1.654655 0.329 26 NDNF 0.746 1.643132 0.246 26TGFB2 0.782 1.633774 0.282 26 GNB3 0.844 1.600635 0.344 26 PTPRD 0.8101.574528 0.310 26 CLTB 0.779 1.568857 0.279 26 PRDM8 0.706 1.5513740.206 26 CAR10 0.758 1.546273 0.258 26 NEUROD4 0.787 1.443959 0.287 26KCNMA1 0.746 1.443881 0.246 26 GABRR1 0.702 1.424760 0.202 26 MAP6 0.7041.389962 0.204 26 CPLX3 0.833 1.368767 0.333 26 CNTNAP2 0.705 1.3573270.205 26 REV3L 0.745 1.315953 0.245 26 HMGN3 0.760 1.309377 0.260 26HSPA12A 0.710 1.264275 0.210 26 CAMSAP2 0.701 1.226712 0.201 26 PPP3CA0.768 1.224280 0.268 26 ANK3 0.715 1.182166 0.215 26 DNAJA1 0.7131.141870 0.213 26 ZFP365 0.701 1.138197 0.201 26 APLP2 0.840 1.1165730.340 26 ATP2B1 0.827 1.109752 0.327 26 2010107E04RIK 0.807 1.0783860.307 26 GLS 0.729 1.030787 0.229 26 MACF1 0.729 1.028031 0.229 26 NRXN30.726 1.013354 0.226 26 ROM1 0.247 −1.535062 0.253 26 CST3 0.258−1.542458 0.242 26 PRPH2 0.199 −1.778911 0.301 26 FAM57B 0.266 −1.8127130.234 26 AIPL1 0.282 −1.854518 0.218 26 PDE6A 0.288 −1.862827 0.212 26NRL 0.236 −1.917565 0.264 26 SLC24A1 0.247 −1.968291 0.253 26 CNGA10.234 −1.993041 0.266 26 NR2E3 0.232 −2.003551 0.268 26 RS1 0.232−2.056603 0.268 26 TULP1 0.179 −2.057501 0.321 26 RP1 0.204 −2.0671140.296 26 GNAT1 0.181 −2.080109 0.319 26 PDE6B 0.199 −2.104653 0.301 26RPGRIP1 0.217 −2.108733 0.283 26 PDE6G 0.180 −2.114659 0.320 26 GNB10.165 −2.145253 0.335 26 RCVRN 0.188 −2.149677 0.312 26 GNGT1 0.146−2.187446 0.354 26 RHO 0.143 −2.216846 0.357 26 SAG 0.133 −2.2852650.367 26 PDC 0.141 −2.289428 0.359 26 cluster no. 27 DE = 27 yDiff myAUCm powe r clus t GRIK1 0.916 3.0 10898 6 2 7 G 0.41 GSG1 0.872 2.6 947182 2 7 0.37 OTOR 0.811 2.5 74650 1 2 7 0.31 NNAT 0.810 2.5 09846 0 2 70.31 FAM19A3 0.808 2.1 90301 8 2 7 FAM 0.30 SLITRK6 0.722 1.9 42192 2 27 SLI 0.22 LHX4 0.775 1.9 30099 5 2 7 0.27 PCP4 0.841 1.6 79884 1 2 70.34 PHYHIPL 0.742 1.6 59067 2 2 7 PHY 0.24 SPHKAP 0.770 1.6 43517 0 2 7SP 0.27 CACNA2D1 1.6 00775 7 2 7 CACN 0.707 0.20 CABP5 0.756 1.5 47771 62 7 C 0.25 SCGN 0.711 1.5 42676 1 2 7 0.21 BC030499 0.704 1.4 55994 4 27 BC03 0.20 LRTM1 0.754 1.4 08952 4 2 7 L 0.25 NME1 0.777 1.3 17789 7 27 0.27 CADPS 0.715 1.2 34166 5 2 7 C 0.21 NEUROD4 0.732 1.2 22587 2 2 7NEU 0.23 VSX2 0.709 1.1 50766 9 2 7 0.20 NRXN3 0.718 1.1 38040 8 2 7 N0.21 APP 0.733 1.1 24188 3 2 7 0.23 PRPH2 0.281 −1.0 16461 9 2 7 P 0.21SAG 0.255 −1.0 43850 5 2 7 0.24 GNAT1 0.289 −1.0 51331 1 2 7 G 0.21RCVRN 0.299 −1.0 59446 1 2 7 R 0.20 PDC 0.261 −1.0 75620 9 2 7 0.23 RHO0.261 −1.0 94430 9 2 7 0.23 myAUC myDiff power cluster # cluster no. 28DE = 48 SLIT2 0.911 2.494784 0.411 28 SCGN 0.910 2.432819 0.410 28 CDH80.874 2.307964 0.374 28 SCG2 0.930 2.181234 0.430 28 ZFHX4 0.8512.178856 0.351 28 VSX1 0.779 1.895571 0.279 28 NETO1 0.751 1.8916870.251 28 GABRA1 0.861 1.787593 0.361 28 PDE1A 0.752 1.652362 0.252 28NEUROD4 0.854 1.610346 0.354 28 GRIA2 0.837 1.599678 0.337 28 CADPS0.828 1.587531 0.328 28 CHRNA6 0.747 1.566433 0.247 28 NTNG1 0.7701.535756 0.270 28 IGF1 0.745 1.475532 0.245 28 TACR3 0.706 1.4660250.206 28 LRTM1 0.810 1.446170 0.310 28 LHX4 0.769 1.437311 0.269 28GRIK1 0.740 1.435103 0.240 28 TNNT1 0.717 1.388436 0.217 28 PTPRD 0.8081.388278 0.308 28 THSD7A 0.765 1.381783 0.265 28 ESAM 0.708 1.3721160.208 28 A730046J19RIK 0.711 1.372055 0.211 28 NRXN3 0.819 1.3404820.319 28 SPHKAP 0.761 1.298899 0.261 28 GLRA1 0.711 1.292095 0.211 28CAR10 0.758 1.238441 0.258 28 BC030499 0.717 1.204192 0.217 28 PGM2L10.735 1.189284 0.235 28 TMEM215 0.713 1.158325 0.213 28 PCP4L1 0.7171.150546 0.217 28 GUCY1B3 0.726 1.146479 0.226 28 CNTN1 0.713 1.1368430.213 28 FRMD3 0.704 1.067778 0.204 28 SAMSN1 0.719 1.063324 0.219 28HMGN3 0.745 1.013834 0.245 28 APP 0.761 1.009757 0.261 28 GNB1 0.281−1.213742 0.219 28 PRPH2 0.262 −1.246574 0.238 28 TULP1 0.270 −1.2559720.230 28 RCVRN 0.288 −1.299880 0.212 28 GNGT1 0.251 −1.319077 0.249 28GNAT1 0.263 −1.357660 0.237 28 SAG 0.220 −1.392674 0.280 28 PDE6G 0.262−1.411349 0.238 28 PDC 0.228 −1.424123 0.272 28 RHO 0.225 −1.4570600.275 28 cluster no. 29 DE = 39 SLIT2 0.817 2.116591 0.317 29 GABRA10.832 2.006228 0.332 29 PCDH17 0.702 1.882124 0.202 29 WLS 0.7081.845341 0.208 29 PCDH10 0.727 1.819161 0.227 29 ZFHX4 0.726 1.7727550.226 29 GLRA1 0.744 1.767981 0.244 29 A730046J19RIK 0.706 1.6646590.206 29 SLC24A3 0.739 1.605346 0.239 29 NRXN3 0.824 1.586941 0.324 29KCNMA1 0.754 1.572355 0.254 29 FAM19A3 0.708 1.512326 0.208 29 CABP50.747 1.504850 0.247 29 TMEM215 0.728 1.483366 0.228 29 PHYHIPL 0.7381.470131 0.238 29 PTPRD 0.786 1.461384 0.286 29 SPHKAP 0.755 1.4539580.255 29 CADPS 0.761 1.431341 0.261 29 MEG3 0.863 1.430565 0.363 29LRTM1 0.754 1.359036 0.254 29 THSD7A 0.703 1.356030 0.203 29 NEUROD40.762 1.294731 0.262 29 NME1 0.772 1.192665 0.272 29 VSX2 0.726 1.1815680.226 29 SCG3 0.707 1.048887 0.207 29 APP 0.718 1.021875 0.218 29 ROM10.288 −1.125274 0.212 29 PDE6B 0.285 −1.189444 0.215 29 RP1 0.293−1.195551 0.207 29 TULP1 0.261 −1.220904 0.239 29 GNB1 0.262 −1.2217260.238 29 PRPH2 0.250 −1.249883 0.250 29 SAG 0.222 −1.257367 0.278 29GNAT1 0.257 −1.311936 0.243 29 RCVRN 0.261 −1.362927 0.239 29 PDC 0.222−1.366220 0.278 29 RHO 0.220 −1.378427 0.280 29 PDE6G 0.248 −1.4288050.252 29 GNGT1 0.220 −1.431648 0.280 29 Diff myAUC my power cluster # gecluster no. 30 DE = 60 NFIA 0.850 2.23 6944 30 NF 0.350 NEUROD4 0.9092.12 5019 30 NEURO 0.409 LHX4 0.870 2.05 9044 30 LH 0.370 EPHA7 0.8051.93 1362 30 EPH 0.305 CABP5 0.825 1.86 8986 30 CAB 0.325 HLF 0.786 1.815451 30 H 0.286 PTPRZ1 0.786 1.75 6697 30 PTPR 0.286 ATP2B1 0.923 1.728502 30 ATP2 0.423 TMEM215 0.810 1.69 9286 30 TMEM2 0.310 CDH9 0.7141.66 4116 30 CD 0.214 LMO4 0.794 1.64 8088 30 LM 0.294 SULF2 0.759 1.644281 30 SUL 0.259 GUCY1A3 0.809 1.60 6336 30 GUCY1 0.309 SYT4 0.797 1.597987 30 SY 0.297 GM4792 0.762 1.58 3695 30 GM47 0.262 GRM6 0.776 1.568053 30 GR 0.276 CAR10 0.794 1.53 4313 30 CAR 0.294 GABRR2 0.714 1.515185 30 GABR 0.214 NDNF 0.753 1.50 7846 30 ND 0.253 NRXN3 0.829 1.505059 30 NRX 0.329 KCNG4 0.701 1.48 2390 30 KCN 0.201 GNAO1 0.862 1.446431 30 GNA 0.362 VIPR2 0.733 1.42 0776 30 VIP 0.233 FRMD3 0.751 1.406949 30 FRM 0.251 SAMSN1 0.748 1.40 4241 30 SAMS 0.248 THSD7A 0.753 1.401838 30 THSD 0.253 SOX4 0.722 1.35 3433 30 SO 0.222 APP 0.808 1.30 803430 A 0.308 GPR179 0.789 1.30 2301 30 GPR1 0.289 TUBB2A 0.781 1.28 151830 TUBB 0.281 LPHN2 0.705 1.26 1045 30 LPH 0.205 PFKP 0.768 1.25 3969 30PF 0.268 ISL1 0.814 1.23 4990 30 IS 0.314 PROX1 0.776 1.21 4681 30 PRO0.276 RRBP1 0.705 1.16 9975 30 RRB 0.205 GABRB3 0.703 1.16 0288 30 GABR0.203 MEIS2 0.709 1.13 1658 30 MEI 0.209 GNG13 0.728 1.09 5088 30 GNG0.228 LIN7A 0.754 1.08 9638 30 LIN 0.254 GRIA2 0.755 1.02 6466 30 GRI0.255 HMGN1 0.256 −1.17 6538 30 HMG 0.244 ROM1 0.290 −1.26 0595 30 RO0.210 RPGRIP1 0.273 −1.55 6331 30 RPGRI 0.227 RS1 0.279 −1.57 7275 30 R0.221 GNGT1 0.219 −1.58 9959 30 GNG 0.281 RP1 0.255 −1.60 4790 30 R0.245 GNB1 0.225 −1.61 1631 30 GN 0.275 NRL 0.272 −1.62 8679 30 N 0.228NR2E3 0.271 −1.64 1338 30 NR2 0.229 CNGA1 0.272 −1.66 4166 30 CNG 0.228PDE6B 0.248 −1.67 9470 30 PDE 0.252 TULP1 0.222 −1.68 8332 30 TUL 0.278PRPH2 0.212 −1.69 0732 30 PRP 0.288 SLC24A1 0.280 −1.69 0999 30 SLC240.220 PDE6G 0.227 −1.72 7951 30 PDE 0.273 SAG 0.180 −1.74 5533 30 S0.320 GNAT1 0.217 −1.75 8815 30 GNA 0.283 RCVRN 0.223 −1.82 2401 30 RCV0.277 PDC 0.186 −1.83 3586 30 P 0.314 RHO 0.180 −1.85 2674 30 R 0.320cluster no. 31 DE = 58 LHX4 0.834 1.94 0702 31 LH 0.334 SCGN 0.830 1.885197 31 SC 0.330 GSG1 0.798 1.78 8603 31 GS 0.298 NEUROD4 0.859 1.760730 31 NEURO 0.359 FRMD3 0.823 1.75 3604 31 FRM 0.323 PCP2 0.899 1.745442 31 PC 0.399 SCG2 0.863 1.69 1052 31 SC 0.363 SPHKAP 0.803 1.68 844731 SPHK 0.303 LPHN2 0.778 1.68 5417 31 LPH 0.278 CABP5 0.752 1.63 673431 CAB 0.252 B3GALT2 0.786 1.61 2381 31 B3GAL 0.286 GUCY1A3 0.797 1.574051 31 GUCY1 0.297 GNG13 0.855 1.57 2693 31 GNG 0.355 LMO4 0.763 1.549801 31 LM 0.263 PTPRZ1 0.720 1.47 1441 31 PTPR 0.220 CDH11 0.701 1.463621 31 CDH 0.201 ST18 0.709 1.46 0354 31 ST 0.209 CAR10 0.772 1.45 546631 CAR 0.272 CADPS 0.770 1.41 8726 31 CAD 0.270 GNB3 0.830 1.41 6090 31GN 0.330 BHLHE23 0.705 1.38 4752 31 BHLHE 0.205 SLC24A3 0.721 1.29 404731 SLC24 0.221 GRM6 0.754 1.28 4539 31 GR 0.254 NRXN3 0.791 1.26 7068 31NRX 0.291 LIN7A 0.768 1.25 5294 31 LIN 0.268 RAB3C 0.710 1.25 1581 31RAB 0.210 PTPRD 0.740 1.23 6538 31 PTP 0.240 ISL1 0.803 1.22 8409 31 IS0.303 PROX1 0.749 1.21 1165 31 PRO 0.249 FAM184A 0.722 1.20 6153 31FAM18 0.222 SAMSN1 0.713 1.20 3743 31 SAMS 0.213 VSX2 0.749 1.19 7906 31VS 0.249 GM4792 0.721 1.14 0953 31 GM47 0.221 GPR179 0.746 1.10 2994 31GPR1 0.246 GUCY1B3 0.703 1.07 1395 31 GUCY1 0.203 KCNMA1 0.708 1.06 261131 KCNM 0.208 CLTB 0.720 1.05 8852 31 CL 0.220 NREP 0.768 1.04 1988 31NR 0.268 NME1 0.766 1.02 1691 31 NM 0.266 TCF4 0.724 1.01 5121 31 TC0.224 ROM1 0.282 −1.31 8723 31 RO 0.218 RPGRIP1 0.290 −1.38 7286 31RPGRI 0.210 RP1 0.260 −1.45 1372 31 R 0.240 TULP1 0.242 −1.47 2154 31TUL 0.258 PRPH2 0.236 −1.47 3241 31 PRP 0.264 NR2E3 0.283 −1.49 2186 31NR2 0.217 CNGA1 0.280 −1.52 3041 31 CNG 0.220 SLC24A1 0.291 −1.57 297231 SLC24 0.209 PDE6B 0.250 −1.62 5189 31 PDE 0.250 NRL 0.274 −1.63 093631 N 0.226 GNB1 0.217 −1.66 5855 31 GN 0.283 RCVRN 0.233 −1.66 8240 31RCV 0.267 RS1 0.266 −1.70 2551 31 R 0.234 PDE6G 0.228 −1.70 7456 31 PDE0.272 GNAT1 0.222 −1.71 8310 31 GNA 0.278 SAG 0.184 −1.74 9072 31 S0.316 RHO 0.185 −1.76 0460 31 R 0.315 PDC 0.188 −1.79 5587 31 P 0.312cluster no. 32 DE = 81 myAUC myDiff power cluster # IGFN1 0.906 2.6094910.406 32 VSX1 0.915 2.599423 0.415 32 GM4792 0.916 2.180753 0.416 32RELN 0.823 2.118713 0.323 32 KCNMA1 0.866 1.893963 0.366 32 GABRR2 0.8251.851548 0.325 32 GNB3 0.904 1.829577 0.404 32 NDNF 0.827 1.827548 0.32732 FN1 0.770 1.821386 0.270 32 TMSB10 0.882 1.803877 0.382 32 GNG130.903 1.777596 0.403 32 HS3ST4 0.749 1.761498 0.249 32 CDH9 0.7461.710895 0.246 32 TRNP1 0.838 1.698429 0.338 32 B3GALT2 0.814 1.6913210.314 32 CADPS 0.842 1.679079 0.342 32 GRM6 0.863 1.668717 0.363 32PTPRD 0.849 1.654509 0.349 32 LRTM1 0.843 1.632109 0.343 32 CABP2 0.7521.631417 0.252 32 NME1 0.885 1.576501 0.385 32 GABRA1 0.816 1.5674860.316 32 GPR179 0.821 1.563361 0.321 32 IGF1 0.781 1.547194 0.281 32ADCY2 0.719 1.544332 0.219 32 NRXN3 0.849 1.526952 0.349 32 THSD7A 0.7861.515832 0.286 32 GRIA2 0.827 1.451331 0.327 32 TTYH1 0.863 1.4342370.363 32 PROX1 0.810 1.418727 0.310 32 GUCY1A3 0.781 1.414072 0.281 32SULF2 0.722 1.410361 0.222 32 BC030499 0.734 1.321296 0.234 32 SNCB0.837 1.317248 0.337 32 SH3BGRL 0.722 1.302330 0.222 32 CAR10 0.7641.297869 0.264 32 FSCN1 0.709 1.288708 0.209 32 4930447C04RIK 0.7371.286988 0.237 32 ASIC3 0.715 1.284343 0.215 32 TMEM215 0.725 1.2827540.225 32 TUBB2A 0.789 1.250102 0.289 32 GNAO1 0.855 1.247950 0.355 32SLC4A10 0.704 1.241247 0.204 32 LPHN2 0.718 1.218956 0.218 32 FRMD30.728 1.173764 0.228 32 ATP2B1 0.855 1.171837 0.355 32 PLK5 0.7561.171749 0.256 32 RIT2 0.715 1.170071 0.215 32 SAMSN1 0.721 1.1641450.221 32 NAP1L5 0.762 1.144805 0.262 32 PCP4L1 0.730 1.119889 0.230 32MYO5A 0.707 1.115274 0.207 32 GLS 0.764 1.097304 0.264 32 GUCY1B3 0.7111.095756 0.211 32 TPI1 0.772 1.082205 0.272 32 MEG3 0.831 1.080701 0.33132 CAMK2B 0.706 1.058614 0.206 32 MIF 0.772 1.047922 0.272 32 TGFB20.737 1.045723 0.237 32 PLCB4 0.724 1.021512 0.224 32 GABRG2 0.7061.011047 0.206 32 HMGN1 0.260 −1.184526 0.240 32 CST3 0.289 −1.3819710.211 32 TULP1 0.239 −1.536871 0.261 32 NRL 0.277 −1.561603 0.223 32RPGRIP1 0.275 −1.597091 0.225 32 SLC24A1 0.276 −1.639280 0.224 32 RP10.250 −1.663774 0.250 32 GNB1 0.206 −1.720470 0.294 32 NR2E3 0.269−1.722247 0.231 32 GNAT1 0.225 −1.727259 0.275 32 CNGA1 0.260 −1.7767490.240 32 PRPH2 0.200 −1.839337 0.300 32 SAG 0.175 −1.845768 0.325 32PDE6G 0.212 −1.904791 0.288 32 PDE6B 0.229 −1.905210 0.271 32 RS1 0.254−1.915177 0.246 32 RCVRN 0.220 −1.923512 0.280 32 GNGT1 0.174 −1.9263940.326 32 RHO 0.175 −1.927010 0.325 32 PDC 0.173 −1.986239 0.327 32cluster no. 33 DE = 47 yDiff myAUC m powe r clus t SCGN 0.832 2.3 885922 3 3 0.33 VSX1 0.785 2.2 63301 5 3 3 0.28 SCG2 0.843 2.1 13311 3 3 30.34 ISL1 0.857 2.0 29040 7 3 3 0.35 CCK 0.706 1.9 93466 6 3 3 0.20 GRM60.817 1.8 09452 7 3 3 0.31 GABRA1 0.805 1.7 68523 5 3 3 GA 0.30 RELN0.729 1.7 64877 9 3 3 0.22 UNC13C 0.726 1.6 81823 6 3 3 UN 0.22 GNG130.837 1.6 70562 7 3 3 G 0.33 FRMD3 0.749 1.6 58409 9 3 3 F 0.24 PTPRZ10.724 1.6 36544 4 3 3 PT 0.22 CADPS 0.757 1.5 04070 7 3 3 C 0.25 TRPM10.848 1.4 72669 8 3 3 T 0.34 BC030499 0.710 1.4 54178 0 3 3 BC03 0.21SAMSN1 0.710 1.3 71458 0 3 3 SA 0.21 NEUROD4 0.750 1.3 61455 0 3 3 NEU0.25 PCP4L1 0.711 1.3 31851 1 3 3 PC 0.21 LRTM1 0.737 1.3 30798 7 3 3 L0.23 APLP2 0.830 1.2 66608 0 3 3 A 0.33 LIN7A 0.740 1.2 23872 0 3 3 L0.24 GNB3 0.765 1.2 19286 5 3 3 0.26 PROX1 0.716 1.2 04813 6 3 3 P 0.21GPR179 0.717 1.1 92149 7 3 3 GP 0.21 HMGN3 0.728 1.1 83215 8 3 3 H 0.22SCG3 0.729 1.1 68200 9 3 3 0.22 MAP4 0.750 1.1 05830 0 3 3 0.25 FAM171B0.711 1.0 92140 1 3 3 FAM 0.21 PTPRD 0.705 1.0 69875 5 3 3 P 0.20 GNAO10.771 1.0 68373 1 3 3 G 0.27 NME1 0.740 1.0 58745 0 3 3 0.24 SLC12A50.703 1.0 03819 3 3 3 SLC 0.20 NRXN3 0.702 1.0 00143 2 3 3 N 0.20 TULP10.293 −1.0 56098 7 3 3 T 0.20 PRPH2 0.250 −1.2 74321 0 3 3 P 0.25 PDE6B0.276 −1.2 80609 4 3 3 P 0.22 RCVRN 0.266 −1.2 86723 4 3 3 R 0.23 NRL0.298 −1.2 87522 2 3 3 0.20 RP1 0.280 −1.2 88988 0 3 3 0.22 NR2E3 0.299−1.2 92005 1 3 3 N 0.20 PDC 0.223 −1.3 61036 7 3 3 0.27 GNGT1 0.226 −1.364027 4 3 3 G 0.27 SAG 0.210 −1.3 86078 0 3 3 0.29 GNAT1 0.246 −1.391683 4 3 3 G 0.25 GNB1 0.240 −1.3 95529 0 3 3 0.26 PDE6G 0.251 −1.409619 9 3 3 P 0.24 RHO 0.213 −1.4 52949 7 3 3 0.28 myAUC myDiff powercluster # cluster no. 34 DE = 147 GLUL 0.983 3.674486 0.483 34 APOE0.984 3.656912 0.484 34 RLBP1 0.972 3.488780 0.472 34 CLU 0.954 3.3002400.454 34 SLC1A3 0.949 3.248626 0.449 34 ACSL3 0.974 3.168933 0.474 34CYR61 0.778 3.161355 0.278 34 CAR14 0.906 3.093884 0.406 34 SPC25 0.9073.027510 0.407 34 COL9A1 0.909 2.992981 0.409 34 JUN 0.836 2.9554120.336 34 DKK3 0.954 2.932319 0.454 34 CP 0.899 2.916545 0.399 34 ID30.858 2.906750 0.358 34 DBI 0.935 2.847955 0.435 34 CRYM 0.889 2.7326410.389 34 HES1 0.812 2.692426 0.312 34 CD9 0.869 2.679822 0.369 34 SPARC0.943 2.675237 0.443 34 FOS 0.791 2.665697 0.291 34 AQP4 0.855 2.6569640.355 34 GPR37 0.875 2.652731 0.375 34 DAPL1 0.852 2.601035 0.352 34 KDR0.861 2.589813 0.361 34 PTN 0.872 2.531457 0.372 34 ZFP36L1 0.7732.523635 0.273 34 TIMP3 0.839 2.505126 0.339 34 ABCA8A 0.830 2.4728550.330 34 MFGE8 0.890 2.441779 0.390 34 PRDX6 0.846 2.426776 0.346 34PDPN 0.813 2.317330 0.313 34 ID2 0.756 2.307350 0.256 34 SIX3OS1 0.8352.306322 0.335 34 DUSP1 0.707 2.262662 0.207 34 SPON1 0.817 2.2378700.317 34 MT1 0.747 2.202169 0.247 34 PPAP2B 0.792 2.196871 0.292 34 ESPN0.807 2.190774 0.307 34 IER2 0.727 2.190246 0.227 34 SAT1 0.786 2.1859230.286 34 CROT 0.798 2.153557 0.298 34 NUDT4 0.848 2.150174 0.348 34CRYAB 0.771 2.112165 0.271 34 VIM 0.814 2.088221 0.314 34 EGR1 0.7482.088219 0.248 34 SOX9 0.740 2.082991 0.240 34 RDH10 0.780 2.0824760.280 34 CAR2 0.913 2.045093 0.413 34 ID1 0.733 2.038664 0.233 34 GNAI20.802 2.032953 0.302 34 VEGFA 0.776 2.021208 0.276 34 NDRG2 0.7912.017386 0.291 34 CDH2 0.817 2.011985 0.317 34 ENPP2 0.740 2.0020790.240 34 FLT1 0.768 1.988472 0.268 34 COL23A1 0.777 1.987731 0.277 34MLC1 0.752 1.962605 0.252 34 FXYD1 0.746 1.938091 0.246 34 TRPM3 0.7681.927747 0.268 34 COX4I2 0.754 1.915573 0.254 34 FXYD6 0.724 1.9119930.224 34 SOX2 0.737 1.898436 0.237 34 TSC22D4 0.763 1.895771 0.263 34E130114P18RIK 0.743 1.893771 0.243 34 PBXIP1 0.739 1.893285 0.239 34GPM6A 0.846 1.881375 0.346 34 DDR1 0.734 1.861470 0.234 34 ATP1B3 0.7501.841852 0.250 34 TGFB2 0.795 1.836747 0.295 34 CAV1 0.718 1.8085740.218 34 CACNG4 0.784 1.804662 0.284 34 UTP14B 0.709 1.801134 0.209 34IL33 0.706 1.782774 0.206 34 SBSPON 0.710 1.779906 0.210 34 KCNJ10 0.7081.778244 0.208 34 VCAM1 0.701 1.776161 0.201 34 GAS1 0.706 1.7708900.206 34 WIPI1 0.754 1.729124 0.254 34 PON2 0.714 1.720217 0.214 34GPM6B 0.823 1.671461 0.323 34 CNN3 0.739 1.664857 0.239 34 RTN4 0.8831.661778 0.383 34 ALDOC 0.803 1.656881 0.303 34 JUND 0.742 1.6431570.242 34 CD63 0.726 1.593887 0.226 34 BSG 0.854 1.587853 0.354 34 SLMAP0.741 1.575019 0.241 34 TIMP2 0.703 1.573740 0.203 34 TTYH1 0.8611.556066 0.361 34 ITM2B 0.852 1.552977 0.352 34 SCD2 0.757 1.5521540.257 34 SYNPR 0.751 1.549654 0.251 34 PAK3 0.718 1.514124 0.218 34OGFRL1 0.738 1.499757 0.238 34 CTSL 0.787 1.492531 0.287 34 RCN2 0.7011.447565 0.201 34 CD81 0.765 1.434966 0.265 34 ATP1A1 0.711 1.4296820.211 34 MARCKS 0.793 1.390002 0.293 34 HTRA1 0.721 1.369298 0.221 34LAPTM4A 0.737 1.348239 0.237 34 ENO1 0.785 1.330226 0.285 34 PFN2 0.7301.324261 0.230 34 SLC16A1 0.727 1.315201 0.227 34 PAX6 0.721 1.2797650.221 34 PRDX1 0.702 1.197453 0.202 34 TCF4 0.738 1.190289 0.238 34CDKN1B 0.722 1.184339 0.222 34 RTN3 0.743 1.050844 0.243 34 MGARP 0.8361.038173 0.336 34 TSPAN3 0.718 1.021941 0.218 34 HSP90AA1 0.234−1.192803 0.266 34 HMGN1 0.196 −1.565337 0.304 34 SLC6A6 0.299 −1.6087740.201 34 MAP1B 0.292 −1.609128 0.208 34 TMA7 0.272 −1.689161 0.228 34STX3 0.298 −1.711322 0.202 34 SYT1 0.269 −1.758105 0.231 34 UNC119 0.221−1.758329 0.279 34 CRX 0.297 −1.766956 0.203 34 CNGB1 0.293 −1.7763280.207 34 SNAP25 0.257 −1.829279 0.243 34 PDE6A 0.287 −1.834439 0.213 34FAM57B 0.261 −1.845724 0.239 34 MPP4 0.298 −1.849733 0.202 34 AIPL10.277 −1.875251 0.223 34 GNB1 0.184 −1.966538 0.316 34 NRL 0.233−1.974974 0.267 34 RS1 0.234 −1.987316 0.266 34 SLC24A1 0.241 −1.9880350.259 34 NEUROD1 0.241 −2.000359 0.259 34 RP1 0.205 −2.033017 0.295 34CNGA1 0.229 −2.048482 0.271 34 RCVRN 0.190 −2.103059 0.310 34 PDE6B0.202 −2.104712 0.298 34 ROM1 0.189 −2.109556 0.311 34 NR2E3 0.226−2.125234 0.274 34 PDE6G 0.178 −2.131050 0.322 34 A930011O12RIK 0.237−2.131781 0.263 34 TULP1 0.171 −2.188185 0.329 34 GNAT1 0.173 −2.1897410.327 34 PDC 0.148 −2.206493 0.352 34 PRPH2 0.159 −2.230242 0.341 34GNGT1 0.140 −2.230657 0.360 34 RHO 0.141 −2.253663 0.359 34 RPGRIP10.210 −2.271849 0.290 34 SAG 0.131 −2.316081 0.369 34 cluster no. 35 DE= 164 IGFBP5 0.980 3.971539 0.480 35 IGF2 0.969 3.900102 0.469 35 PTN0.967 3.682716 0.467 35 S100B 0.935 3.590062 0.435 35 PDGFRA 0.9353.318071 0.435 35 CST3 0.999 3.249334 0.499 35 APOE 0.969 2.946241 0.46935 ALDOC 0.949 2.788765 0.449 35 CTGF 0.840 2.723195 0.340 35 ID3 0.8912.635791 0.391 35 SPARC 0.977 2.633834 0.477 35 MLC1 0.882 2.6328860.382 35 NTRK2 0.878 2.607959 0.378 35 RGS5 0.854 2.582399 0.354 35 DBI0.929 2.569035 0.429 35 CNTNAP2 0.890 2.499012 0.390 35 1500015O10RIK0.759 2.470979 0.259 35 GFAP 0.796 2.454143 0.296 35 ATP1A2 0.8822.442214 0.382 35 LECT1 0.820 2.435971 0.320 35 CP 0.888 2.423026 0.38835 PPAP2B 0.858 2.381629 0.358 35 SLC1A3 0.873 2.359476 0.373 35 CD90.882 2.341085 0.382 35 FXYD6 0.856 2.288842 0.356 35 SCD2 0.8782.195817 0.378 35 CLU 0.938 2.194379 0.438 35 CXCL12 0.822 2.1560660.322 35 SLC4A4 0.809 2.154664 0.309 35 ITM2B 0.960 2.154164 0.460 35SLC30A10 0.812 2.149123 0.312 35 CLEC18A 0.731 2.137565 0.231 35 TIMP30.815 2.122132 0.315 35 CRIM1 0.804 2.079012 0.304 35 SLC6A11 0.7992.061326 0.299 35 PRDX6 0.828 2.056543 0.328 35 GLUL 0.902 2.0397920.402 35 IGFBP2 0.762 2.038345 0.262 35 CLDN10 0.759 2.007019 0.259 35TSC22D4 0.805 1.983938 0.305 35 CRIP1 0.784 1.981687 0.284 35 GPM6B0.894 1.956617 0.394 35 CD36 0.713 1.930346 0.213 35 MGST1 0.7931.926971 0.293 35 MGLL 0.813 1.906835 0.313 35 SPON1 0.794 1.9039750.294 35 MT1 0.762 1.901464 0.262 35 FN1 0.742 1.898765 0.242 35 CGNL10.727 1.886294 0.227 35 EPAS1 0.769 1.878394 0.269 35 DDAH1 0.8311.877818 0.331 35 PAM 0.815 1.876076 0.315 35 VIM 0.816 1.805763 0.31635 TGFB2 0.824 1.793167 0.324 35 PDLIM3 0.744 1.782440 0.244 35 NPC20.807 1.762614 0.307 35 PDPN 0.798 1.757502 0.298 35 CTSL 0.856 1.7468570.356 35 ID2 0.770 1.744332 0.270 35 LAPTM4A 0.810 1.727350 0.310 35 B2M0.749 1.719217 0.249 35 FXYD1 0.774 1.684176 0.274 35 MT3 0.756 1.6555930.256 35 GJA1 0.748 1.648157 0.248 35 1810037I17RIK 0.781 1.644679 0.28135 LCAT 0.731 1.627679 0.231 35 ID4 0.760 1.626869 0.260 35 CMTM5 0.7481.625331 0.248 35 MMD2 0.807 1.619960 0.307 35 GPX8 0.733 1.614363 0.23335 AGT 0.754 1.613099 0.254 35 AP1S2 0.734 1.593596 0.234 35 CTSD 0.7551.587762 0.255 35 PMP22 0.715 1.581249 0.215 35 CNN3 0.768 1.5501850.268 35 TRPM3 0.720 1.527377 0.220 35 CD81 0.805 1.514989 0.305 35TMEM47 0.743 1.510235 0.243 35 SNED1 0.725 1.495801 0.225 35 NDRG2 0.7661.486505 0.266 35 CDH13 0.708 1.469163 0.208 35 JUN 0.742 1.464296 0.24235 HES1 0.739 1.463197 0.239 35 SERPINH1 0.739 1.457804 0.239 35 QK0.771 1.444155 0.271 35 BCAN 0.731 1.443889 0.231 35 ANXA5 0.7231.441585 0.223 35 ABHD4 0.735 1.440876 0.235 35 PAX8 0.704 1.4242040.204 35 PLA2G16 0.703 1.398253 0.203 35 6330403K07RIK 0.718 1.3879640.218 35 RCN1 0.711 1.387198 0.211 35 FBXO2 0.723 1.385921 0.223 35CRYAB 0.713 1.384143 0.213 35 ITGB1 0.743 1.382103 0.243 35 MAP4K4 0.7401.374146 0.240 35 METRN 0.721 1.367026 0.221 35 CTNNBIP1 0.730 1.3647000.230 35 ATP1A1 0.763 1.364599 0.263 35 CNTN1 0.742 1.359653 0.242 35APPL2 0.720 1.347765 0.220 35 TCEAL3 0.756 1.330603 0.256 35 NFIA 0.7051.316319 0.205 35 MYO6 0.743 1.310000 0.243 35 SOX2 0.709 1.306380 0.20935 LSAMP 0.731 1.294332 0.231 35 BTBD3 0.701 1.285695 0.201 35 NFIB0.726 1.284242 0.226 35 SPARCL1 0.774 1.275405 0.274 35 CD63 0.7121.268344 0.212 35 TSPAN3 0.826 1.263679 0.326 35 SOX9 0.725 1.2631360.225 35 SYT11 0.710 1.252546 0.210 35 DKK3 0.819 1.250533 0.319 35 ADD30.761 1.231412 0.261 35 OGFRL1 0.710 1.229288 0.210 35 TES 0.7011.187409 0.201 35 DAD1 0.715 1.143170 0.215 35 CDH2 0.744 1.142469 0.24435 APP 0.767 1.135626 0.267 35 GNAS 0.806 1.122998 0.306 35 BSG 0.7721.113302 0.272 35 PSAP 0.756 1.094708 0.256 35 LMAN1 0.753 1.0894730.253 35 CRIP2 0.718 1.082840 0.218 35 LAMP1 0.751 1.065592 0.251 35LAMP2 0.715 1.045180 0.215 35 SORBS2 0.703 1.035769 0.203 35 SIX3 0.7331.025975 0.233 35 SEPT2 0.722 1.024609 0.222 35 PAK3 0.703 1.0160540.203 35 LRPAP1 0.709 1.015462 0.209 35 D4WSU53E 0.293 −1.205302 0.20735 HSP90AA1 0.233 −1.301165 0.267 35 HMGN1 0.214 −1.515951 0.286 35UNC119 0.265 −1.543727 0.235 35 TMA7 0.282 −1.609110 0.218 35 RS1 0.258−1.739989 0.242 35 EPB4.1 0.294 −1.784873 0.206 35 ROM1 0.228 −1.7952560.272 35 SNAP25 0.269 −1.797526 0.231 35 A930011O12RIK 0.269 −1.8043490.231 35 RP1 0.237 −1.805896 0.263 35 NRL 0.269 −1.838217 0.231 35 NR2E30.251 −1.864726 0.249 35 GNB1 0.199 −1.937908 0.301 35 PRPH2 0.189−1.965544 0.311 35 CNGA1 0.249 −1.979693 0.251 35 NEUROD1 0.257−1.983968 0.243 35 CNGB1 0.290 −1.997218 0.210 35 RCVRN 0.209 −2.0103920.291 35 RPGRIP1 0.236 −2.027461 0.264 35 SYT1 0.262 −2.027895 0.238 35GNAT1 0.203 −2.043737 0.297 35 PDE6A 0.291 −2.060641 0.209 35 TULP10.203 −2.069090 0.297 35 FAM57B 0.254 −2.158818 0.246 35 PDE6B 0.206−2.203795 0.294 35 PDE6G 0.188 −2.230095 0.312 35 SLC24A1 0.245−2.235394 0.255 35 PDC 0.159 −2.252119 0.341 35 GNGT1 0.151 −2.2773440.349 35 RHO 0.143 −2.360853 0.357 35 SAG 0.138 −2.476095 0.362 35cluster no. 36 DE = 153 OPTC 0.947 4.425130 0.447 36 CRHBP 0.9643.776445 0.464 36 ATP1A2 0.951 3.648260 0.451 36 COL9A1 0.976 3.5540070.476 36 PTGDS 0.915 3.501014 0.415 36 COL18A1 0.946 3.487830 0.446 36GJA1 0.923 3.420054 0.423 36 FBLN1 0.906 3.182397 0.406 36 IGFBP2 0.8853.142612 0.385 36 PTN 0.915 3.008914 0.415 36 PENK 0.787 2.989587 0.28736 CP 0.950 2.984993 0.450 36 FBN2 0.911 2.956232 0.411 36 DAPL1 0.8632.902905 0.363 36 SNED1 0.879 2.890684 0.379 36 FSTL1 0.908 2.8670430.408 36 APOE 0.978 2.824762 0.478 36 PVRL3 0.899 2.796596 0.399 36SPARC 0.956 2.740817 0.456 36 FBN1 0.858 2.736953 0.358 36 TIMP3 0.8942.725876 0.394 36 ATP1B3 0.887 2.707483 0.387 36 COL23A1 0.899 2.6182790.399 36 DKK3 0.960 2.573613 0.460 36 RELN 0.859 2.549885 0.359 36TSC22D1 0.901 2.516971 0.401 36 APP 0.951 2.481702 0.451 36 MFAP4 0.8292.416559 0.329 36 NTRK2 0.858 2.412425 0.358 36 MEST 0.869 2.4073660.369 36 LTBP1 0.846 2.364761 0.346 36 VCAN 0.805 2.364323 0.305 36 OGN0.794 2.342607 0.294 36 FAM129A 0.805 2.301763 0.305 36 ALDH1A1 0.7712.278916 0.271 36 COL9A2 0.808 2.241696 0.308 36 IQGAP2 0.797 2.2164830.297 36 NBL1 0.810 2.211997 0.310 36 MFAP2 0.807 2.209952 0.307 36IGFBP7 0.829 2.206748 0.329 36 MDK 0.795 2.178341 0.295 36 COL2A1 0.7922.165488 0.292 36 ZIC1 0.775 2.152048 0.275 36 TMPRSS11E 0.747 2.1389060.247 36 RHOJ 0.813 2.116804 0.313 36 TRPM3 0.813 2.116794 0.313 36COL9A3 0.788 2.116159 0.288 36 NUDT4 0.864 2.107740 0.364 36 FMOD 0.7762.038997 0.276 36 BMP4 0.764 2.005755 0.264 36 SFRP1 0.775 2.0037350.275 36 SLC6A13 0.740 1.996986 0.240 36 SLC13A4 0.759 1.992519 0.259 36WFDC1 0.745 1.992328 0.245 36 CTSL 0.889 1.973272 0.389 36 SERPINH10.797 1.970538 0.297 36 LTBP3 0.776 1.954298 0.276 36 PKP4 0.7781.935166 0.278 36 CCND2 0.733 1.887738 0.233 36 HTRA1 0.778 1.8841200.278 36 MGST1 0.756 1.883879 0.256 36 FOLR1 0.750 1.882648 0.250 36COL4A5 0.756 1.862932 0.256 36 CPQ 0.756 1.838248 0.256 36 GAS1 0.7441.835410 0.244 36 CTSD 0.841 1.824145 0.341 36 OCIAD2 0.741 1.8189160.241 36 LIPA 0.746 1.818661 0.246 36 ZIC4 0.711 1.807990 0.211 36LAPTM4A 0.849 1.799329 0.349 36 SGK1 0.742 1.797747 0.242 36 B3GALTL0.760 1.785010 0.260 36 OLFML2A 0.723 1.760141 0.223 36 CD63 0.7611.734796 0.261 36 TGFB2 0.798 1.720278 0.298 36 CGN 0.735 1.702379 0.23536 BMP2 0.729 1.701840 0.229 36 LRP1 0.733 1.697547 0.233 36 SDC2 0.7571.685581 0.257 36 TKT 0.792 1.652767 0.292 36 GLDC 0.725 1.644414 0.22536 CLDN19 0.741 1.636605 0.241 36 TNFRSF21 0.714 1.626433 0.214 36COL11A1 0.723 1.621136 0.223 36 TENM4 0.743 1.620626 0.243 36 NFIB 0.7611.612994 0.261 36 VIM 0.779 1.590580 0.279 36 GNG11 0.717 1.589828 0.21736 CTSH 0.716 1.586077 0.216 36 CNTN1 0.733 1.583022 0.233 36 HES1 0.7571.576002 0.257 36 SHISA2 0.736 1.573728 0.236 36 MAB21L2 0.752 1.5490830.252 36 DEFB9 0.706 1.541091 0.206 36 ILDR2 0.709 1.510602 0.209 36GPX8 0.716 1.484254 0.216 36 PAM 0.736 1.479638 0.236 36 ABI3BP 0.7111.477928 0.211 36 CD59A 0.728 1.450541 0.228 36 PODXL2 0.765 1.4346510.265 36 SLC41A1 0.710 1.434087 0.210 36 CD81 0.780 1.424905 0.280 36CLU 0.795 1.422895 0.295 36 SLC6A6 0.827 1.411126 0.327 36 PAX6 0.7521.379180 0.252 36 MT-ND6 0.709 1.365749 0.209 36 MT-ND5 0.839 1.3640840.339 36 PLXNB2 0.701 1.363449 0.201 36 FLRT1 0.703 1.311944 0.203 36TMEM176B 0.705 1.288783 0.205 36 SDC4 0.741 1.282822 0.241 36 BSG 0.7921.276199 0.292 36 GM26924 0.759 1.260216 0.259 36 MT-ND2 0.832 1.2316830.332 36 RRBP1 0.721 1.223343 0.221 36 SLC2A1 0.725 1.220867 0.225 36CAR14 0.716 1.170677 0.216 36 CD47 0.717 1.167718 0.217 36 PDIA3 0.7271.157075 0.227 36 GLUL 0.810 1.149020 0.310 36 RCN2 0.716 1.108386 0.21636 MT-ND4 0.810 1.009844 0.310 36 SYT1 0.291 −1.338995 0.209 36 HSP90AA10.202 −1.484852 0.298 36 RS1 0.240 −1.616647 0.260 36 CNGA1 0.263−1.629758 0.237 36 SNAP25 0.279 −1.656418 0.221 36 HMGN1 0.195 −1.6724250.305 36 PDE6A 0.293 −1.773595 0.207 36 GNB1 0.208 −1.790238 0.292 36SLC24A1 0.246 −1.800033 0.254 36 AIPL1 0.285 −1.800568 0.215 36 UNC1190.225 −1.801700 0.275 36 A930011O12RIK 0.250 −1.828064 0.250 36 ROM10.211 −1.886096 0.289 36 NEUROD1 0.245 −1.893158 0.255 36 FAM57B 0.258−1.960973 0.242 36 NR2E3 0.238 −1.986178 0.262 36 PDE6B 0.210 −2.0239970.290 36 MGARP 0.241 −2.025761 0.259 36 RPGRIP1 0.225 −2.056657 0.275 36CNGB1 0.284 −2.060958 0.216 36 NRL 0.235 −2.076837 0.265 36 TULP1 0.187−2.098105 0.313 36 RP1 0.204 −2.140954 0.296 36 GNGT1 0.151 −2.1445350.349 36 RCVRN 0.203 −2.146519 0.297 36 PDC 0.153 −2.195983 0.347 36 RHO0.143 −2.197936 0.357 36 PDE6G 0.185 −2.223749 0.315 36 GNAT1 0.181−2.279163 0.319 36 SAG 0.133 −2.287358 0.367 36 PRPH2 0.165 −2.2988660.335 36 cluster no. 37 DE = 236 IGFBP7 0.980 3.838996 0.480 37 CLDN50.944 3.452232 0.444 37 RGS5 0.778 3.413786 0.278 37 PTPRB 0.9383.322368 0.438 37 SPARCL1 0.977 3.260195 0.477 37 SPARC 0.985 3.2226770.485 37 ITM2A 0.928 3.082648 0.428 37 COL4A1 0.923 3.047394 0.423 37ELTD1 0.934 3.005777 0.434 37 LY6C1 0.843 2.932233 0.343 37 CTLA2A 0.8832.913169 0.383 37 PLTP 0.880 2.911192 0.380 37 FLT1 0.945 2.907156 0.44537 FN1 0.895 2.874017 0.395 37 CD93 0.896 2.763199 0.396 37 RAMP2 0.9002.687166 0.400 37 BSG 0.959 2.670912 0.459 37 SEPP1 0.867 2.663650 0.36737 GPR116 0.888 2.662459 0.388 37 FAM101B 0.869 2.611442 0.369 37 MGP0.747 2.598253 0.247 37 COL4A2 0.884 2.569211 0.384 37 EGFL7 0.8612.554202 0.361 37 SLCO1A4 0.819 2.547434 0.319 37 TMSB4X 0.958 2.5380770.458 37 LY6E 0.880 2.518953 0.380 37 SPOCK2 0.887 2.484721 0.387 37GNG11 0.852 2.460344 0.352 37 SLC7A5 0.832 2.450158 0.332 37 CD34 0.8492.334600 0.349 37 VWA1 0.836 2.320906 0.336 37 ITGB1 0.848 2.3178700.348 37 ABCB1A 0.837 2.296619 0.337 37 TM4SF1 0.819 2.273045 0.319 37PECAM1 0.833 2.249158 0.333 37 LAMA4 0.840 2.246115 0.340 37 CDH5 0.8432.239309 0.343 37 ETS1 0.824 2.194360 0.324 37 SLCO1C1 0.775 2.1750530.275 37 SERPINH1 0.825 2.169857 0.325 37 ESAM 0.825 2.149808 0.325 37SLC16A1 0.835 2.128338 0.335 37 AU021092 0.815 2.116002 0.315 37 SLC2A10.871 2.108619 0.371 37 KLF2 0.782 2.108125 0.282 37 NRP1 0.794 2.0927600.294 37 IFITM3 0.800 2.075435 0.300 37 MFSD2A 0.771 2.062993 0.271 37ENG 0.803 2.050977 0.303 37 LAMB1 0.794 2.044396 0.294 37 GNAI2 0.8582.034857 0.358 37 CALD1 0.771 2.033018 0.271 37 APOD 0.731 2.0143400.231 37 B2M 0.807 2.012573 0.307 37 TPM4 0.812 2.011884 0.312 37TSC22D1 0.865 1.988874 0.365 37 NID1 0.786 1.988835 0.286 37 AHNAK 0.7701.972169 0.270 37 MYL12A 0.799 1.968519 0.299 37 HTRA3 0.785 1.9666200.285 37 KDR 0.851 1.957857 0.351 37 VIM 0.825 1.918437 0.325 37 MYH90.792 1.914794 0.292 37 ECE1 0.810 1.899870 0.310 37 EPAS1 0.7901.873475 0.290 37 LY6A 0.714 1.841976 0.214 37 FOXQ1 0.774 1.8406020.274 37 TEK 0.756 1.838929 0.256 37 NES 0.766 1.837284 0.266 37 ECSCR0.750 1.827206 0.250 37 PALMD 0.770 1.814667 0.270 37 SLC7A1 0.7571.765044 0.257 37 ACTB 0.956 1.764859 0.456 37 RGCC 0.731 1.760596 0.23137 MSN 0.775 1.756457 0.275 37 PTRF 0.750 1.756409 0.250 37 ANXA3 0.7671.756155 0.267 37 BC028528 0.764 1.746908 0.264 37 VWF 0.738 1.7296670.238 37 SLC9A3R2 0.747 1.721684 0.247 37 FZD6 0.758 1.719270 0.258 37ANXA2 0.762 1.715881 0.262 37 SLC39A10 0.752 1.715856 0.252 37 TIE10.748 1.715698 0.248 37 PPIC 0.754 1.692879 0.254 37 KITL 0.723 1.6881310.223 37 APLNR 0.730 1.686510 0.230 37 PLXND1 0.731 1.679477 0.231 37SRGN 0.750 1.678497 0.250 37 CRIP2 0.780 1.677601 0.280 37 SPTBN1 0.8651.671355 0.365 37 RRBP1 0.798 1.669390 0.298 37 SLC39A8 0.726 1.6656690.226 37 LTBP4 0.715 1.659100 0.215 37 ARPC1B 0.754 1.646160 0.254 37CSRP2 0.769 1.644461 0.269 37 FLI1 0.748 1.643560 0.248 37 AGRN 0.7691.641418 0.269 37 ARL4A 0.765 1.635757 0.265 37 TCF4 0.826 1.6306060.326 37 CLEC14A 0.724 1.627629 0.224 37 RASIP1 0.742 1.626477 0.242 37APP 0.858 1.625496 0.358 37 CTNNB1 0.815 1.624392 0.315 37 ARHGAP290.757 1.621671 0.257 37 RHOB 0.765 1.620359 0.265 37 MYO1B 0.7441.616759 0.244 37 KANK3 0.738 1.614200 0.238 37 ITGA1 0.739 1.6007120.239 37 UACA 0.745 1.596853 0.245 37 CDKN1A 0.737 1.596169 0.237 37NFKBIA 0.767 1.588506 0.267 37 LMO2 0.739 1.587364 0.239 37 ABLIM1 0.8171.586307 0.317 37 TPM3-RS7 0.753 1.572490 0.253 37 CTSH 0.736 1.5604860.236 37 ID3 0.798 1.551172 0.298 37 SLC3A2 0.803 1.550705 0.303 37ITGA6 0.721 1.549646 0.221 37 ABCG2 0.719 1.534372 0.219 37 EMCN 0.7341.531817 0.234 37 TMEM252 0.712 1.530900 0.212 37 PTPRG 0.737 1.5207040.237 37 TAGLN2 0.736 1.519652 0.236 37 S1PR1 0.730 1.512398 0.230 37SDPR 0.706 1.511013 0.206 37 UTRN 0.727 1.510283 0.227 37 SLC40A1 0.7251.509780 0.225 37 ID1 0.737 1.507196 0.237 37 CD200 0.755 1.505153 0.25537 EOGT 0.710 1.504481 0.210 37 PLS3 0.716 1.490015 0.216 37 ATOX1 0.7811.479614 0.281 37 HSPG2 0.709 1.475721 0.209 37 CGNL1 0.724 1.4700550.224 37 RHOC 0.718 1.454245 0.218 37 ADAM10 0.752 1.454056 0.252 37CYB5R3 0.744 1.446513 0.244 37 GIMAP6 0.708 1.440910 0.208 37 LAPTM4A0.788 1.437107 0.288 37 ZFP36L1 0.757 1.431819 0.257 37 FOXP1 0.7281.428272 0.228 37 GNB4 0.709 1.426711 0.209 37 LRRC58 0.804 1.4264170.304 37 WWTR1 0.733 1.425046 0.233 37 LSR 0.717 1.424805 0.217 37 REEP30.734 1.421046 0.234 37 CNN2 0.719 1.419514 0.219 37 ANXA5 0.7201.413657 0.220 37 RHOJ 0.724 1.411383 0.224 37 H2-D1 0.720 1.4100030.220 37 CLIC4 0.725 1.395593 0.225 37 PFN1 0.761 1.389536 0.261 37ACTN4 0.759 1.381403 0.259 37 MYO10 0.759 1.373926 0.259 37 ROBO4 0.7041.372148 0.204 37 TMSB10 0.793 1.367258 0.293 37 CLIC1 0.710 1.3568320.210 37 ABHD2 0.706 1.345547 0.206 37 PTBP3 0.704 1.338826 0.204 37LEF1 0.706 1.336777 0.206 37 LAMC1 0.704 1.334944 0.204 37 S100A13 0.7021.331773 0.202 37 RBMS1 0.704 1.324417 0.204 37 GPCPD1 0.736 1.3113590.236 37 RALB 0.706 1.301303 0.206 37 TPM3 0.740 1.300676 0.240 37LIMCH1 0.727 1.300556 0.227 37 QK 0.738 1.296033 0.238 37 MAOA 0.7031.294644 0.203 37 LRP8 0.711 1.293956 0.211 37 NFIB 0.713 1.286120 0.21337 FERMT2 0.723 1.282462 0.223 37 SERINC3 0.766 1.277661 0.266 37 TPM10.733 1.268704 0.233 37 OSTF1 0.712 1.264445 0.212 37 PODXL 0.7381.258107 0.238 37 DOCK9 0.706 1.254311 0.206 37 PPFIBP1 0.702 1.2477570.202 37 SELM 0.718 1.243887 0.218 37 IQGAP1 0.718 1.237155 0.218 37NOTCH1 0.701 1.224235 0.201 37 WASF2 0.701 1.195270 0.201 37 KLF6 0.7031.182019 0.203 37 RAC1 0.723 1.178323 0.223 37 HES1 0.708 1.178252 0.20837 SYNM 0.715 1.159417 0.215 37 HIP1 0.712 1.133942 0.212 37 ARPC3 0.7051.129207 0.205 37 GPX1 0.718 1.126453 0.218 37 TNFAIP1 0.702 1.1260670.202 37 ACTN1 0.703 1.105354 0.203 37 MYH10 0.715 1.105079 0.215 37CAPNS1 0.712 1.100011 0.212 37 HSP90AB1 0.823 1.063223 0.323 37 ITM2B0.775 1.046377 0.275 37 CTNNA1 0.735 1.045557 0.235 37 ARPC5 0.7141.035917 0.214 37 ARPC2 0.741 1.002383 0.241 37 GNB2 0.709 1.0006950.209 37 CD2AP 0.705 1.000147 0.205 37 GNB1 0.250 −1.474782 0.250 37TMA7 0.293 −1.657448 0.207 37 HSP90AA1 0.188 −1.688760 0.312 37 ANP32E0.287 −1.782614 0.213 37 HMGN1 0.187 −1.810023 0.313 37 EPB4.1 0.297−1.825915 0.203 37 CNGA1 0.245 −1.839320 0.255 37 CRX 0.298 −1.8566250.202 37 CKB 0.258 −1.875027 0.242 37 SNAP25 0.270 −1.886785 0.230 37PDE6A 0.291 −1.892818 0.209 37 NEUROD1 0.252 −1.945246 0.248 37 SYT10.264 −1.950146 0.236 37 AIPL1 0.279 −1.961332 0.221 37 UNC119 0.213−1.984213 0.287 37 FAM57B 0.260 −1.996296 0.240 37 RS1 0.242 −1.9981380.258 37 MGARP 0.241 −2.018440 0.259 37 ROM1 0.207 −2.054687 0.293 37RCVRN 0.204 −2.079733 0.296 37 GNAT1 0.187 −2.113967 0.313 37 NRL 0.235−2.122317 0.265 37 SLC24A1 0.248 −2.125249 0.252 37 RP1 0.211 −2.1360680.289 37 PRPH2 0.177 −2.140244 0.323 37 PDE6B 0.206 −2.170048 0.294 37NR2E3 0.229 −2.230401 0.271 37 PDE6G 0.181 −2.259370 0.319 37 TULP10.177 −2.260649 0.323 37 PDC 0.154 −2.296981 0.346 37 RHO 0.144−2.311761 0.356 37 A930011O12RIK 0.240 −2.318021 0.260 37 GNGT1 0.142−2.329702 0.358 37 SAG 0.136 −2.357981 0.364 37 RPGRIP1 0.210 −2.4844760.290 37 cluster no. 38 DE = 147 RGS5 0.992 5.501167 0.492 38 MGP 0.9924.465241 0.492 38 IGFBP7 0.966 4.035969 0.466 38 COL4A1 0.974 3.6321990.474 38 CALD1 0.989 3.427224 0.489 38 COL4A2 0.925 3.164541 0.425 38ATP1A2 0.916 3.153645 0.416 38 SERPINE2 0.867 3.078251 0.367 38 ASPN0.904 3.066492 0.404 38 KCNJ8 0.801 2.949732 0.301 38 ABCC9 0.8252.914127 0.325 38 ITGA1 0.880 2.901163 0.380 38 NID1 0.887 2.8658950.387 38 MYL9 0.848 2.784330 0.348 38 SPARCL1 0.921 2.771803 0.421 38HIGD1B 0.841 2.751780 0.341 38 FSTL1 0.836 2.746793 0.336 38 ITGB1 0.8432.690748 0.343 38 ITIH5 0.713 2.661303 0.213 38 GNG11 0.837 2.6497340.337 38 COL1A2 0.814 2.596983 0.314 38 COL3A1 0.785 2.565582 0.285 38PDGFRB 0.856 2.494842 0.356 38 GJC1 0.829 2.453495 0.329 38 TM4SF1 0.7682.425629 0.268 38 CRIP1 0.720 2.420014 0.220 38 IFITM3 0.799 2.4134640.299 38 CSPG4 0.761 2.403481 0.261 38 SPARC 0.940 2.383060 0.440 38MYO1B 0.795 2.250938 0.295 38 MYL12A 0.804 2.246027 0.304 38 SERPINH10.794 2.240935 0.294 38 MCAM 0.768 2.235239 0.268 38 ART3 0.769 2.2250340.269 38 CASQ2 0.730 2.198628 0.230 38 LAMA4 0.752 2.197344 0.252 38LAMB1 0.765 2.179149 0.265 38 TPM4 0.786 2.173681 0.286 38 CD248 0.7692.172865 0.269 38 TPM1 0.728 2.168649 0.228 38 LAMC1 0.806 2.1523520.306 38 ETS1 0.744 2.113024 0.244 38 GJA4 0.714 2.090454 0.214 38 TIMP30.753 2.075556 0.253 38 CFH 0.713 2.068239 0.213 38 EDNRA 0.777 2.0414610.277 38 NDUFA4L2 0.790 2.032572 0.290 38 SEPT7 0.903 2.026055 0.403 38EBF1 0.805 2.024674 0.305 38 PTRF 0.720 2.024501 0.220 38 NOTCH3 0.7222.014656 0.222 38 SEPT11 0.798 2.003902 0.298 38 PLAT 0.750 2.0025670.250 38 S1PR3 0.755 1.999823 0.255 38 UACA 0.729 1.995204 0.229 38 MYH90.760 1.981694 0.260 38 RGS4 0.741 1.980531 0.241 38 FLNA 0.708 1.9797510.208 38 NAALAD2 0.753 1.962642 0.253 38 S100A11 0.743 1.951513 0.243 38NRP1 0.785 1.946284 0.285 38 SEPT4 0.805 1.932384 0.305 38 BGN 0.7451.895552 0.245 38 PPIC 0.751 1.881210 0.251 38 PCDH18 0.743 1.8661560.243 38 MAGED2 0.752 1.849301 0.252 38 CNN2 0.721 1.848057 0.221 38NBL1 0.737 1.837023 0.237 38 MARCKS 0.837 1.808142 0.337 38 VIM 0.7451.769597 0.245 38 ARHGDIB 0.705 1.769381 0.205 38 B2M 0.735 1.7640190.235 38 ADAP2 0.706 1.740003 0.206 38 EPAS1 0.760 1.738220 0.260 38NR2F2 0.741 1.729772 0.241 38 UTRN 0.712 1.709004 0.212 38 ID3 0.7371.706232 0.237 38 GUCY1A3 0.798 1.705109 0.298 38 ACTB 0.929 1.6852650.429 38 LAPTM4A 0.815 1.676642 0.315 38 RHOB 0.727 1.667873 0.227 38RBMS1 0.708 1.644134 0.208 38 LRRC58 0.827 1.640398 0.327 38 MEF2C 0.7121.640375 0.212 38 CCDC80 0.713 1.628830 0.213 38 ANXA5 0.715 1.5841200.215 38 ITM2B 0.851 1.582958 0.351 38 FERMT2 0.705 1.565111 0.205 38CD63 0.718 1.561257 0.218 38 MFGE8 0.772 1.548767 0.272 38 WLS 0.7021.535632 0.202 38 MPRIP 0.725 1.530097 0.225 38 SERINC3 0.738 1.5145500.238 38 SLC12A2 0.722 1.511126 0.222 38 LHFP 0.701 1.509888 0.201 38GINM1 0.703 1.495549 0.203 38 CD81 0.819 1.485171 0.319 38 VTN 0.7351.473185 0.235 38 APP 0.793 1.469747 0.293 38 RAC1 0.714 1.426087 0.21438 TNFAIP1 0.705 1.405605 0.205 38 OAZ2 0.706 1.349629 0.206 38 NREP0.759 1.298044 0.259 38 PTEN 0.719 1.252699 0.219 38 TMSB4X 0.7721.138718 0.272 38 SPTBN1 0.716 1.048742 0.216 38 LAMP1 0.737 1.0392900.237 38 D4WSU53E 0.298 −1.146991 0.202 38 SNAP25 0.296 −1.457235 0.20438 HSP90AA1 0.203 −1.509721 0.297 38 MGARP 0.250 −1.523003 0.250 38NEUROD1 0.277 −1.532473 0.223 38 HMGN1 0.188 −1.744434 0.312 38 SLC24A10.267 −1.817590 0.233 38 TMA7 0.271 −1.832750 0.229 38 FAM57B 0.267−1.841072 0.233 38 SYT1 0.265 −1.845972 0.235 38 CRX 0.292 −1.8769620.208 38 ELOVL4 0.297 −1.878393 0.203 38 CKB 0.250 −1.883214 0.250 38UNC119 0.220 −1.904351 0.280 38 NDUFA4 0.220 −1.957810 0.280 38 MPP40.295 −1.968298 0.205 38 AIPL1 0.278 −1.972794 0.222 38 EPB4.1 0.279−2.013098 0.221 38 GNB1 0.192 −2.027415 0.308 38 NR2E3 0.232 −2.0989910.268 38 1810009A15RIK 0.291 −2.121394 0.209 38 PDE6G 0.188 −2.1414900.312 38 PDE6A 0.274 −2.163994 0.226 38 NRL 0.233 −2.193383 0.267 38CNGB1 0.282 −2.220351 0.218 38 RS1 0.227 −2.230808 0.273 38 TULP1 0.179−2.310206 0.321 38 CNGA1 0.225 −2.318757 0.275 38 RCVRN 0.188 −2.3190520.312 38 RP1 0.201 −2.341225 0.299 38 RHO 0.153 −2.379167 0.347 38RPGRIP1 0.215 −2.390692 0.285 38 PDC 0.147 −2.404465 0.353 38A930011O12RIK 0.231 −2.444744 0.269 38 GNAT1 0.174 −2.450650 0.326 38SAG 0.140 −2.497791 0.360 38 PDE6B 0.194 −2.533895 0.306 38 PRPH2 0.151−2.581111 0.349 38 ROM1 0.175 −2.590215 0.325 38 GNGT1 0.133 −2.6602610.367 38 cluster no. 39 DE = 153 CTSS 0.978 4.653922 0.478 39 HEXB 0.9764.292110 0.476 39 C1QB 0.970 3.878037 0.470 39 C1QC 0.948 3.834225 0.44839 APOE 0.962 3.754892 0.462 39 C1QA 0.948 3.723967 0.448 39 CCL4 0.7543.720710 0.254 39 B2M 0.938 3.647541 0.438 39 CX3CR1 0.903 3.5205500.403 39 LY86 0.903 3.481497 0.403 39 P2RY12 0.880 3.398210 0.380 39CCL3 0.791 3.365822 0.291 39 SEPP1 0.916 3.341246 0.416 39 CSF1R 0.8953.191319 0.395 39 LAPTM5 0.903 3.170011 0.403 39 ZFP36 0.875 3.1544730.375 39 TYROBP 0.873 3.084486 0.373 39 JUNB 0.862 3.023664 0.362 39NFKBIA 0.805 3.015364 0.305 39 KLF2 0.729 2.944302 0.229 39 SIGLECH0.880 2.904145 0.380 39 ATF3 0.751 2.874536 0.251 39 TREM2 0.8512.847238 0.351 39 JUN 0.901 2.800797 0.401 39 CTSD 0.895 2.785069 0.39539 RHOB 0.863 2.668613 0.363 39 SGK1 0.791 2.595234 0.291 39 FCER1G0.820 2.594593 0.320 39 SELPLG 0.791 2.583273 0.291 39 MPEG1 0.8062.561161 0.306 39 TMSB4X 0.978 2.518332 0.478 39 GPR34 0.776 2.4846800.276 39 SERPINE2 0.851 2.447607 0.351 39 SPARC 0.906 2.436520 0.406 39GRN 0.813 2.425319 0.313 39 IER5 0.773 2.410207 0.273 39 NPC2 0.8322.385903 0.332 39 LGMN 0.952 2.385703 0.452 39 KLF6 0.744 2.379144 0.24439 LYZ2 0.746 2.374372 0.246 39 EGR1 0.834 2.333774 0.334 39 FCGR3 0.7762.313824 0.276 39 RGS2 0.803 2.307229 0.303 39 4632428N05RIK 0.7682.250471 0.268 39 CTSZ 0.821 2.233623 0.321 39 CST3 0.964 2.231930 0.46439 ITGAM 0.752 2.200036 0.252 39 ACTB 0.956 2.193357 0.456 39 FYB 0.7732.190362 0.273 39 TGFBR1 0.766 2.176746 0.266 39 KCTD12 0.757 2.1695580.257 39 UNC93B1 0.746 2.159913 0.246 39 AIF1 0.754 2.148845 0.254 39CYBA 0.759 2.143158 0.259 39 MAFB 0.725 2.130408 0.225 39 CTSB 0.9002.106910 0.400 39 H2-D1 0.755 2.100278 0.255 39 DUSP1 0.721 2.0843360.221 39 RNASE4 0.716 2.084032 0.216 39 SERINC3 0.830 2.075356 0.330 39PTGS1 0.739 2.071713 0.239 39 FCRLS 0.746 2.055869 0.246 39 UBC 0.8342.024625 0.334 39 LAIR1 0.737 2.014039 0.237 39 H2-K1 0.719 2.0138170.219 39 CTSL 0.887 2.003522 0.387 39 LY6E 0.764 2.000438 0.264 39 ITGB50.740 1.998945 0.240 39 PSAP 0.854 1.998267 0.354 39 SAT1 0.739 1.9975780.239 39 LTC4S 0.731 1.992351 0.231 39 ARPC1B 0.736 1.989627 0.236 39MARCKS 0.877 1.984915 0.377 39 CD53 0.716 1.979296 0.216 39 LRRC58 0.8771.965416 0.377 39 APBB1IP 0.709 1.956031 0.209 39 BTG2 0.755 1.9552860.255 39 PLEK 0.711 1.946862 0.211 39 RGS10 0.737 1.924107 0.237 39 IER20.721 1.912803 0.221 39 PLXDC2 0.738 1.910001 0.238 39 F11R 0.7141.890608 0.214 39 IRF8 0.701 1.868279 0.201 39 PLD4 0.731 1.865511 0.23139 CTSA 0.754 1.835910 0.254 39 FOS 0.723 1.826721 0.223 39 MAF 0.7141.823466 0.214 39 ITM2B 0.917 1.811843 0.417 39 CD9 0.765 1.806437 0.26539 IFNGR1 0.742 1.805089 0.242 39 JUND 0.756 1.804582 0.256 39 LPCAT20.767 1.791338 0.267 39 CTSH 0.725 1.784451 0.225 39 MERTK 0.7061.779292 0.206 39 TRF 0.720 1.778704 0.220 39 CD81 0.808 1.768962 0.30839 CLIC1 0.711 1.731795 0.211 39 RRBP1 0.751 1.708872 0.251 39 GPX10.731 1.694199 0.231 39 MSN 0.704 1.650198 0.204 39 CREG1 0.725 1.6412350.225 39 TPM3-RS7 0.702 1.631400 0.202 39 LAMP2 0.704 1.522471 0.204 39TIMP2 0.705 1.496183 0.205 39 QK 0.707 1.462699 0.207 39 FTH1 0.8531.383409 0.353 39 TPM3 0.707 1.355049 0.207 39 LAMP1 0.743 1.2747440.243 39 RPS9 0.740 1.227865 0.240 39 GM9843 0.764 1.151216 0.264 39RPL32 0.759 1.139049 0.259 39 RPS26 0.720 1.130727 0.220 39 RPLP1 0.8011.070725 0.301 39 ANP32A 0.299 −1.167042 0.201 39 HSP90AA1 0.239−1.203183 0.261 39 LDHA 0.291 −1.203661 0.209 39 PKM 0.295 −1.2775400.205 39 NDUFA4 0.273 −1.304189 0.227 39 MAP1B 0.294 −1.335660 0.206 39SYT1 0.285 −1.366615 0.215 39 FAM57B 0.292 −1.413749 0.208 39 NRL 0.279−1.427076 0.221 39 ROM1 0.235 −1.486101 0.265 39 ANP32E 0.287 −1.5045560.213 39 TULP1 0.220 −1.539643 0.280 39 SLC25A4 0.273 −1.541158 0.227 39MGARP 0.256 −1.541918 0.244 39 CPE 0.268 −1.556102 0.232 39 TMA7 0.277−1.583630 0.223 39 SNAP25 0.275 −1.599132 0.225 39 PDE6G 0.205 −1.6602030.295 39 RS1 0.254 −1.663552 0.246 39 PRPH2 0.191 −1.751501 0.309 39RCVRN 0.213 −1.764180 0.287 39 GNAT1 0.205 −1.772742 0.295 39 SLC24A10.261 −1.776117 0.239 39 EPB4.1 0.280 −1.821400 0.220 39 PDE6A 0.290−1.837114 0.210 39 GNGT1 0.172 −1.846910 0.328 39 NEUROD1 0.248−1.869328 0.252 39 UNC119 0.209 −1.871789 0.291 39 A930011O12RIK 0.254−1.877904 0.246 39 STX3 0.288 −1.894001 0.212 39 CNGA1 0.243 −1.9050850.257 39 HMGN1 0.165 −1.905216 0.335 39 NR2E3 0.237 −1.943295 0.263 39RHO 0.166 −1.984178 0.334 39 GNB1 0.182 −2.006714 0.318 39 PDC 0.163−2.033191 0.337 39 PDE6B 0.205 −2.102541 0.295 39 RPGRIP1 0.221−2.105338 0.279 39 SAG 0.154 −2.197799 0.346 39 RP1 0.197 −2.3591180.303 39

Table 7. Differential gene expression between each pairwise combinationof the 39 retinal cell clusters.

TABLE 9Oligonucleotide sequences used in the preparation of Drop-Seq libraries.“B” designates any base but “A”, “J”designates a split-and-pool synthesis round; “N”designates a degenerate base. “*” designates a phosphorothioatelinkage. All soluble primers were purchased from Integrated DNA Technolo-gies, and purified by standard desalting except for the Template_Switch_Oligo, which was purified by ion-exchange-HPLC. Table discloses SEQ IDNOS: 2-16, respectively, in order of appearance. synRNArCrCrUrArCrArCrCrArCrCrCrUrCrUrUrCrCrCrArUrCrUrNrNrNrNrNrNrNrNrNrNrNrNrNrNrNrNrNrNrNrBrArArArArArArArArArArArArArArArArArArArArArArArA Barcoded Bead5′-Bead-Linker-TTTTTTTAAGCAGTGGTATCAACGCAGAGTACGTJJJJJJJJ SeqAJJJJNNNNNNNNTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT-3′ Barcoded Bead5′-Bead-Linker-TTTTTTTAAGCAGTGGTATCAACGCAGAGTACJJJJJJJJJJ SeqBJJNNNNNNNNTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT-3′ Template_Switch_AAGCAGTGGTATCAACGCAGAGTGAATrGrGrG Oligo TSO_PCR AAGCAGTGGTATCAACGCAGAGTP5-TSO_HybridAATGATACGGCGACCACCGAGATCTACACGCCTGTCCGCGGAAGCAGTGGTATCAACGC AGAGT*A*CNextera_N701 CAAGCAGAAGACGGCATACGAGATTCGCCTTAGTCTCGTGGGCTCGGNextera_N702 CAAGCAGAAGACGGCATACGAGATCTAGTACGGTCTCGTGGGCTCGGNextera_N703 CAAGCAGAAGACGGCATACGAGATTTCTGCCTGTCTCGTGGGCTCGGRead1 CustomSeqA GCCTGTCCGCGGAAGCAGTGGTATCAACGCAGAGTACGTRead1 CustomSeqB GCCTGTCCGCGGAAGCAGTGGTATCAACGCAGAGTAC P7-TSO_HybridCAAGCAGAAGACGGCATACGAGATCGTGATCGGTCTCGGCGGAAGCAGTGGTATCAAC GCAGAGT*A*CTruSeq_F AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATC*TCustSynRNASeq CGGTCTCGGCGGAAGCAGTGGTATCAACGCAGAGTAC UMI_SMARTdTAAGCAGTGGTATCAACGCAGAGTACNNNNNNNNNTTTTTTTTTTTTTTTTTTTTTTTT

TABLE 10 “Out of sample” projection test. For each cluster, the“training” cells were removed from the tSNE plot, and then projectedonto the tSNE. The number of cells that successfully project into theembedding, and the number of cells that become inappropriatelyincorporated into a different cluster were tabulated. Cluster # Cells in# failed to # Wrongly % Wrongly # Cluster project # Projected AssignedAssigned 1 153 153 0 0 0.00 2 271 271 0 0 0.00 3 201 201 0 0 0.00 4 4646 0 0 0.00 5 63 62 1 0 0.00 6 173 156 17 9 5.20 7 277 272 5 5 1.81 8115 115 0 0 0.00 9 275 275 0 0 0.00 10 155 153 2 2 1.29 11 165 162 3 31.82 12 175 175 0 0 0.00 13 46 40 6 5 10.87 14 89 89 0 0 0.00 15 52 44 86 11.54 16 179 179 0 0 0.00 17 284 284 0 0 0.00 18 64 63 1 1 1.56 19 108107 1 0 0.00 20 206 206 0 0 0.00 21 154 154 0 0 0.00 22 180 180 0 0 0.0023 183 182 1 1 0.55 24 3712 3417 295 180 4.85 25 1095 1071 24 18 1.64 261213 1212 1 0 0.00 27 323 318 5 4 1.24 28 339 330 9 7 2.06 29 332 324 86 1.81 30 447 426 21 18 4.03 31 346 340 6 3 0.87 32 235 233 2 2 0.85 33453 450 3 3 0.66 34 784 784 0 0 0.00 35 27 27 0 0 0.00 36 43 43 0 0 0.0037 145 139 6 5 3.45 38 30 30 0 0 0.00 39 17 17 0 0 0.00

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The invention is further described by the following numbered paragraphs:

-   1. A nucleotide- or oligonucleotide-adorned bead wherein said bead    comprises:

(a) a linker;

(b) an identical sequence for use as a sequencing priming site;

(c) a uniform or near-uniform nucleotide or oligonucleotide sequence;

(d) a Unique Molecular Identifier which differs for each priming site;

(e) optionally an oligonucleotide redudant sequence for capturingpolyadenylated mRNAs and priming reverse transcription; and optionallyat least one other oligonucleotide barcode which provides an additionalsubstrate for identification.

-   2. The nucleotide- or oligonucleotide-adorned bead of paragraph 1    wherein the nucleotide or oligonucleotide sequence on the surface of    the bead is a molecular barcode.-   3. The nucleotide- or oligonucleotide-adorned bead of paragraph 2    wherein the barcode ranges from 4 to 1000 nucleotides in length.-   4. The nucleotide- or oligonucleotide-adorned bead according to    paragraph 1 wherein the oligonucleotide sequence for capturing    polyadenylated mRNAs and priming reverse transcription is an oligo    dT sequence.-   5. The nucleotide- or oligonucleotide-adorned bead according to    paragraph 1 wherein the linker is a non-cleavable, straight-chain    polymer.-   6. The nucleotide- or oligonucleotide-adorned bead according to    paragraph 1 wherein the linker is a chemically-cleavable,    straight-chain polymer.-   7. The nucleotide- or oligonucleotide-adorned bead according to    paragraph 1 wherein the linker is a non-cleavable optionally    substituted hydrocarbon polymer.-   8. The nucleotide- or oligonucleotide-adorned bead according to    paragraph 1 wherein the linker is a photolabile optionally    substituted hydrocarbon polymer.-   9. The nucleotide- or oligonucleotide-adorned bead according to    paragraph 1 wherein the linker is a polyethylene glycol.-   10. The nucleotide- or oligonucleotide-adorned bead according to    paragraph 1 wherein the linker is a PEG-C₃ to PEG-₂₄.-   11. A mixture comprising a plurality of nucleotide- or    oligonucleotide- adorned beads, wherein said beads comprises:

(a) a linker;

(b) an identical sequence for use as a sequencing priming site;

(c) a uniform or near-uniform nucleotide or oligonucleotide sequence;

(d) a Unique Molecular Identifier which differs for each priming site;

(e) an oligonucleotide redudant sequence for capturing polyadenylatedmRNAs and priming reverse transcription; and

optionally at least one additional oligonucleotide sequences, whichprovide substrates for downstream molecular-biological reactions;

wherein the uniform or near-uniform nucleotide or oligonucleotidesequence is the same across all the priming sites on any one bead, butvaries among the oligonucleotides on an individual bead.

-   12. The mixture of paragraph 11 wherein the nucleotide or    oligonucleotide sequence on the surface of the bead is a molecular    barcode.-   13. The mixture of paragraph 12 wherein the barcode ranges from 4 to    1000 nucleotides in length.-   14. The mixture of paragraph 11 wherein the oligonucleotide sequence    for capturing polyadenylated mRNAs and priming reverse transcription    is an oligo dT sequence.-   15. The mixture of paragraph 11 which comprises at least one    oligonucleotide sequences, which provide for substrates for    downstream molecular-biological reactions.-   16. The mixture of paragraph 11 wherein the downstream molecular    biological reactions are for reverse transcription of mature mRNAs;    capturing specific portions of the transcriptome, priming for DNA    polymerases and/or similar enzymes; or priming throughout the    transcriptome or genome.-   17. The mixture of paragraph 11 wherein the additional    oligonucleotide sequence comprises a oligio-dT sequence.-   18. The mixture of paragraph 11 wherein the additional    oligonucleotide sequence comprises a primer sequence.-   19. The mixture of paragraph 11 wherein the additional    oligonucleotide sequence comprises a oligio-dT sequence and a primer    sequence.-   20. An error-correcting barcode bead wherein said bead comprises:

(a) a linker;

(b) an identical sequence for use as a sequencing priming site;

(c) a uniform or near-uniform nucleotide or oligonucleotide sequencewhich comprises at least a nucleotide base duplicate;

(d) a Unique Molecular Identifier which differs for each priming site;and

(e) an an oligonucleotide redudant for capturing polyadenylated mRNAsand priming reverse transcription;

-   21. A method wherein the barcode beads of paragraph 20 fail to    hybridize to the mRNA thereby failing to undergo reverse    transcription.-   22. A kit which comprises a mixture of oligonucleotide bound beads    of paragraph 1 and self-correcting barcode beads of paragraph 20.-   23. A method for creating a composite single-cell sequencing library    comprising:

(a) merging one uniquely barcoded RNA capture microbead with asingle-cell in an emulsion droplet having a diameter from 50 μm to 210μm;

(b) lysing the cell thereby capturing the RNA on the RNA capturemicrobead;

(c) performing a reverse transcription reaction to convert the cells'RNA to first strand cDNA that is covalently linked to the RNA capturemicrobead; or conversely reverse transcribing within droplets andthereafter breaking droplets and collecting cDNA-attached beads;

(d) preparing and sequencing a single composite RNA-Seq library,containing cell barcodes that record the cell-of-origin of each RNA, andmolecular barcodes that distinguish among RNAs from the same cell.

-   24. A method for creating a composite single-cell sequencing library    comprising:

(a) merging one uniquely barcoded RNA capture microbead with asingle-cell in an emulsion droplet having a diameter from 50 μm to 210μm;

(b) lysing the cell thereby capturing the RNA on the RNA capturemicrobead;

(c) breaking droplets and pooling beads in solution;

(d) performing a reverse transcription reaction to convert the cells'RNA to first strand cDNA that is covalently linked to the RNA capturemicrobead; or conversely reverse transcribing within droplets andthereafter breaking droplets and collecting cDNA-attached beads;

(e) preparing and sequencing a single composite RNA-Seq library,containing cell barcodes that record the cell-of-origin of each RNA, andmolecular barcodes that distinguish among RNAs from the same cell.

-   25. The method of paragraph 23 or paragraph 24, wherein the method    of amplifying the cDNA-attached beads is template switch    amplification.-   26. The method of paragraph 23 or paragraph 24, wherein the method    of amplifying the cDNA-attached beads is T7 linear application.-   27. The method of paragraph 23 or paragraph 24, wherein the method    of amplifying the cDNA-attached beads is exponential isothermal    amplification.-   28. The method of paragraph 23 or paragraph 24, wherein the emulsion    droplet is formed via co-encapsulation comprising RNA capture    microbead and composite single-cell.-   29. The method of paragraph 25 wherein the emulsion droplet is at    least 1.25 to times more than the volume of the RNA capture    microbead.-   30. The method of paragraph 29 wherein the emulsion droplet is at    least 1.5 times the volume of the RNA capture microbead.-   31. The method of paragraph 23 or paragraph 24, wherein the RNA is    mRNA.-   32. The method of paragraph 23 or paragraph 24 wherein the diameter    of the emulsion droplet is 125 μm.-   33. The method of paragraph 23 or paragraph 24 wherein the diameter    of the RNA capture microbeads is from 10 μm to 95 μm.-   34. A method for preparing a plurality of beads with unique nucleic    acid sequence comprising:

(a) performing polynucleotide synthesis on the surface of the pluralityof beads in a pool-and-split process, such that in each cycle ofsynthesis the beads are split into a plurality of subsets wherein eachsubset is subjected to different chemical reactions;

(b) repeating the pool-and-split process from anywhere from 2 cycles to200 cycles.

-   35. The method of paragraph 34 wherein the polynucleotide synthesis    is phosphoramidite synthesis.-   36. The method of paragraph 34 wherein the polynucleotide synthesis    is reverse direction phosphoramidite chemistry.-   37. The method of paragraph 34 wherein each subset is subjected to a    different nucleotide.-   38. The method of paragraph 34 wherein each subset is subjected to a    different canonical nucleotide.-   39. The method of paragraph 34 is repeated three times.-   40. The method of paragraph 34 is repeated four times.-   41. The method of paragraph 34 is repeated twelve times.-   42. The method of paragraph 34, wherein the linker covalently    connecting the microbead to the oligonucleotide is polyethylene    glycol.-   43. The method of any one of paragraphs 34 through 42, wherein the    diameter of the RNA capture microbeads is from 10 μm to 95 μm.-   44. The method of any one of paragraphs 34 through 42 wherein    multiple steps is twelve steps.-   45. A method for simultaneously preparing a plurality of nucleotide-    or oligonucleotide-adorned beads wherein a uniform, near-uniform, or    patterned nucleotide or oligonucleotide sequence is synthesized upon    any individual bead while vast numbers of different nucleotide or    oligonucleotide sequences are simultaneously synthesized on    different beads, comprising:

(a) forming a mixture comprising a plurality of beads;

(b) separating the beads into subsets;

(c) extending the nucleotide or oligonucleotide sequence on the surfaceof the beads by adding an individual nucleotide via chemical synthesis;

(d) pooling the subsets of beads in (c) into a single common pool;

(e) repeating steps (b), (c) and (d) multiple times to produce acombinatorially a thousand or more nucleotide or oligonucleotidesequences; and collecting the nucleotide- or oligonucleotide-adornedbeads.

-   46. The method of paragraph 45 wherein the nucleotide or    oligonucleotide sequence on the surface of the bead is a molecular    barcode.-   47. The method of paragraph 45 wherein the pool-and-split synthesis    steps occur every 2-10 cycles, rather than every cycle.-   48. The method of paragraph 45 wherein the barcode contains built-in    error correction.-   49. The method of paragraph 45 wherein the barcode ranges from 4 to    1000 nucleotides in length.-   50. The method of paragraph 45 wherein the polynucleotide synthesis    is phosphoramidite synthesis.-   51. The method of paragraph 45 wherein the polynucleotide synthesis    is reverse direction phosphoramidite chemistry.-   52. The method of paragraph 45 wherein each subset is subjected to a    different nucleotide.-   53. The method of paragraph 45 further comprising wherein one or    more subsets receive a cocktail of two nucleotides.-   54. The method of paragraph 45 wherein each subset is subjected to a    different canonical nucleotide.-   55. The method of paragraph 45 wherein the bead is a microbead.-   56. The method of paragraph 45 wherein the bead is a nanoparticle.-   57. The method of paragraph 45 wherein the bead is a macrobead.-   58. The method of paragraph 45 where the oligonucleotide sequence is    a dinucleotide.-   59. The method of paragraph 45 where the oligonucleotide sequence is    a trinucleotide.-   60. A method for simultaneously preparing a thousand or more    nucleotide- or oligonucleotide-adorned beads wherein a uniform or    near-uniform nucleotide or oligonucleotide sequence is synthesized    upon any individual bead while a plurality of different nucleotide    or oligonucleotide sequences are simultaneously synthesized on    different beads, comprising:

(a) forming a mixture comprising a plurality of beads;

(b) separating the beads into subsets;

(c) extending the nucleotide or oligonucleotide sequence on the surfaceof the beads by adding an individual nucleotide via chemical synthesis;

(d) pooling the subsets of beads in (c) into a single common pool;

(e) repeating steps (b), (c) and (d) multiple times to produce acombinatorially large number of nucleotide or oligonucleotide sequences;and collecting the nucleotide- or oligonucleotide-adorned beads;

(g) performing polynucleotide synthesis on the surface of the pluralityof beads in a pool-and-split synthesis, such that in each cycle ofsynthesis the beads are split into a plurality of subsets wherein eachsubset is subjected to different chemical reactions;

(h) repeating the pool-and-split synthesis multiple times.

-   61. The method of paragraph 60 wherein the nucleotide or    oligonucleotide sequence on the surface of the bead is a molecular    barcode.-   62. The method of paragraph 60 wherein the pool-and-split synthesis    steps occur every 2-10 cycles, rather than every cycle.-   63. The method of paragraph 60 wherein the generated barcode    contains built-in error correction.-   64. The method of paragraph 60 wherein the barcode ranges from 4 to    1000 nucleotides in length.-   65. The method of paragraph 60 wherein the polynucleotide synthesis    is phosphoramidite synthesis.-   66. The method of paragraph 60 wherein the polynucleotide synthesis    is reverse direction phosphoramidite chemistry.-   67. The method of paragraph 60 wherein each subset is subjected to a    different nucleotide.-   68. The method of paragraph 60 further comprising wherein one or    more subsets receive a cocktail of two nucleotides.-   69. The method of paragraph 60 wherein each subset is subjected to a    different canonical nucleotide.-   70. The method of paragraph 60 wherein the bead is a microbead.-   71. The method of paragraph 60 wherein the bead is a nanoparticle.-   72. The method of paragraph 60 wherein the bead is a macrobead.-   73. The method of paragraph 60 where the oligonucleotide barcoded    bead is a dinucleotide.-   74. The method of paragraph 60 where the oligonucleotide barcoded    bead is a trinucleotide.-   75. The method of paragraph 45 or paragraph 60 wherein the    pool-and-split synthesis is repeated twelve times.-   76. The method of paragraph 45 or paragraph 60 wherein the diameter    of the complexed bead is from 10 μm to 95 μm.-   77. An apparatus for creating a composite single-cell sequencing    library via a microfluidic system, comprising:

a oil-surfactant inlet comprising a filter and a carrier fluid channel,wherein said carrier fluid channel further comprises a resistor;

an inlet for an analyte comprising a filter and a carrier fluid channel,wherein said carrier fluid channel further comprises a resistor;

an inlet for mRNA capture microbeads and lysis reagent comprising afilter and a carrier fluid channel, wherein said carrier fluid channelfurther comprises a resistor;

said carrier fluid channels have a carrier fluid flowing therein at anadjustable or predetermined flow rate;

wherein each said carrier fluid channels merge at a junction; and saidjunction being connected to a mixer, which contains an outlet for drops.

-   78. The apparatus of paragraph 77, wherein the analyte comprises a    chemical reagent, a protein, a drug, an antibody, an enzyme, a    nucleic acid, an organelle, a cell or any combination thereof.-   79. The apparatus of paragraph 77 wherein said junction is connected    to said mixer by a fluid carrier channel with a constriction for    droplet pinch-off.-   80. The apparatus of paragraph 77, wherein the analyte is a cell.-   81. The apparatus of paragraph 77, wherein the analyte is a    mammalian cell.-   82. The apparatus of paragraph 77, wherein the analyte is complex    tissue.-   83. The apparatus of paragraph 81, wherein the cell is a brain cell.-   84. The apparatus of paragraph 81, wherein the cell is a retina    cell.-   85. The apparatus of paragraph 81, wherein the cell is a human bone    marrow cell.-   86. The apparatus of paragraph 81, wherein the cell is a    host-pathogen cell.-   87. The apparatus of paragraph 77, wherein the lysis reagent    comprises an anionic surfactant, such as sodium lauroyl sarcosine,    or a chaotropic salt, such as guanidiunium thiocyanate.-   88. The apparatus of paragraph 77, wherein the filter comprises    square PDMS.-   89. The apparatus of paragraph 77, wherein the resistor is    serpentine having a length from 7000-9000, width of 50-75 μm and    depth of 100-150 mm.-   90. The resistor of paragraph 89, which has a diameter of 50 μm.-   91. The apparatus of paragraph 77, wherein the channels having a    length of length of 8000-12,000 μm and width of 125-250 mm, and    depth of 100-150 mm.-   92. The channel of paragraph 89, wherein the diameter is 125 μm.-   93. The apparatus of paragraph 77, wherein the mixer has a length of    7000-9000 μm and a width of 110-140 μm.-   94. The mixer of paragraph 93, wherein the width is 125 μm.-   95. The apparatus of paragraph 77, wherein the oil-surfactant is a    PEG block polymer.-   96. The apparatus of paragraph 95, wherein the PEG block polymer is    BIORADTM QX200 Droplet Generation Oil.-   97. The apparatus of paragraph 77, wherein the carrier fluid is    water-glycerol mixture.

Having thus described in detail preferred embodiments of the presentinvention, it is to be understood that the invention defined by theabove paragraphs is not to be limited to particular details set forth inthe above description as many apparent variations thereof are possiblewithout departing from the spirit or scope of the present invention.

1-97. (canceled) Please add the following claims:
 98. A nucleotide- oroligonucleotide-adorned bead wherein said bead comprises: (a) a linker;(b) an identical sequence for use as a sequencing priming site; (c) auniform or near-uniform nucleotide or oligonucleotide sequence; (d) aUnique Molecular Identifier which differs for each priming site; (e)optionally an oligonucleotide redudant sequence for capturingpolyadenylated mRNAs and priming reverse transcription; and (f)optionally at least one other oligonucleotide barcode which provides anadditional substrate for identification.
 99. The nucleotide- oroligonucleotide-adorned bead of claim 98, wherein: the nucleotide oroligonucleotide sequence on the surface of the bead is a molecularbarcode; or the nucleotide or oligonucleotide sequence on the surface ofthe bead is a molecular barcode from 4 to 1000 nucleotides in length; orthe oligonucleotide sequence for capturing polyadenylated mRNAs andpriming reverse transcription is an oligo dT sequence; or the linker isa non-cleavable, straight-chain polymer; or the linker is achemically-cleavable, straight-chain polymer; or the linker is anon-cleavable optionally substituted hydrocarbon polymer; or the linkeris a photolabile optionally substituted hydrocarbon polymer; or thelinker is a polyethylene glycol; or the linker is a PEG-C₃₋₂₄.
 100. Amixture comprising a plurality of nucleotide- or oligonucleotide-adorned beads, wherein said beads comprises; (a) a linker; (b) anidentical sequence for use as a sequencing priming site; (c) a uniformor near-uniform nucleotide or oligonucleotide sequence; (d) a UniqueMolecular Identifier which differs for each priming site; (e) anoligonucleotide redudant sequence for capturing polyadenylated mRNAs andpriming reverse transcription; and (f) optionally at least oneadditional oligonucleotide sequences which provide substrates fordownstream molecular-biological reactions; wherein the uniform ornear-uniform nucleotide or oligonucleotide sequence is the same acrossall the priming sites on any one bead, but varies among theoligonucleotides on an individual bead.
 101. The mixture of claim 100,wherein the nucleotide or oligonucleotide sequence on the surface of thebead is a molecular barcode; of wherein the nucleotide oroligonucleotide sequence on the surface of the bead is a molecularbarcode from 4 to 1000 nucleotides in length; or wherein theoligonucleotide sequence for capturing polyadenylated mRNAs and primingreverse transcription is an oligo dT sequence; or which comprises atleast one oligonucleotide sequences, which provide for substrates fordownstream molecular-biological reactions; or wherein the downstreammolecular biological reactions are for reverse transcription of maturemRNAs; capturing specific portions of the transcriptome, priming for DNApolymerases and/or similar enzymes; or priming throughout thetranscriptome or genome; or wherein the additional oligonucleotidesequence comprises a oligio-dT sequence; or wherein the additionaloligonucleotide sequence comprises a primer sequence; or wherein theadditional oligonucleotide sequence comprises a oligio-dT sequence and aprimer sequence.
 102. An error-correcting barcode bead wherein said beadcomprises: (a) a linker; (b) an identical sequence for use as asequencing priming site; (c) a uniform or near-uniform nucleotide oroligonucleotide sequence which comprises at least a nucleotide baseduplicate; (d) a Unique Molecular Identifier which differs for eachpriming site; and (e) an oligonucleotide redudant for capturingpolyadenylated mRNAs and priming reverse transcription;
 103. A methodwherein the barcode beads of claim 102, fail to hybridize to the mRNAthereby failing to undergo reverse transcription.
 104. A kit whichcomprises a mixture of oligonucleotide bound beads of claim 1 andself-correcting barcode beads of claim 102..
 105. A method for creatinga composite single-cell sequencing library comprising: (a) merging oneuniquely barcoded RNA capture microbead with a single-cell in anemulsion droplet having a diameter from 50 μm to 210 μm; (b) lysing thecell thereby capturing the RNA on the RNA capture microbead; (c)performing a reverse transcription reaction to convert the cells' RNA tofirst strand cDNA that is covalently linked to the RNA capturemicrobead; or conversely reverse transcribing within droplets andthereafter breaking droplets and collecting cDNA-attached beads; (d)preparing and sequencing a single composite RNA-Seq library, containingcell barcodes that record the cell-of-origin of each RNA, and molecularbarcodes that distinguish among RNAs from the same cell.
 106. A methodfor creating a composite single-cell sequencing library comprising: (a)merging one uniquely barcoded RNA capture microbead with a single-cellin an emulsion droplet having a diameter from 50 μm to 210 μm; (b)lysing the cell thereby capturing the RNA on the RNA capture microbead;(c) breaking droplets and pooling beads in solution; (d) performing areverse transcription reaction to convert the cells' RNA to first strandcDNA that is covalently linked to the RNA capture microbead; orconversely reverse transcribing within droplets and thereafter breakingdroplets and collecting cDNA-attached beads; (e) preparing andsequencing a single composite RNA-Seq library, containing cell barcodesthat record the cell-of-origin of each RNA, and molecular barcodes thatdistinguish among RNAs from the same cell.
 107. The method of claim 106,wherein the method of amplifying the cDNA-attached beads is templateswitch amplification; or the method of amplifying the cDNA-attachedbeads is T7 linear application; or the method of amplifying thecDNA-attached beads is exponential isothermal amplification; or theemulsion droplet is formed via co-encapsulation comprising RNA capturemicrobead and composite single-cell; or the emulsion droplet is at least1.25 μm; or the diameter of the RNA capture microbeads is from 10 μm to95 μm.
 108. A method for preparing a plurality of beads with uniquenucleic acid sequence comprising: (a) performing polynucleotidesynthesis on the surface of the plurality of beads in a pool-and-splitprocess, such that in each cycle of synthesis the beads are split into aplurality of subsets wherein each subset is subjected to differentchemical reactions; (b) repeating the pool-and-split process fromanywhere from 2 cycles to 200 cycles.
 109. The method of claim 108,wherein the polynucleotide synthesis is phosphoramidite synthesis; orthe polynucleotide synthesis is reverse direction phosphoramiditechemistry; or each subset is subjected to a different nucleotide; oreach subset is subjected to a different canonical nucleotide; or themethod is repeated three times; or the method is repeated four times; orthe method is repeated twelve times; or the linker covalently connectingthe microbead to the oligonucleotide is polyethylene glycol.
 110. Themethod of claim 109, wherein the diameter of the RNA capture microbeadsis from 10 μm to 95 μm; or multiple steps is twelve steps.
 111. A methodfor simultaneously preparing a plurality of nucleotide- oroligonucleotide-adorned beads wherein a uniform, near-uniform, orpatterned nucleotide or oligonucleotide sequence is synthesized upon anyindividual bead while vast numbers of different nucleotide oroligonucleotide sequences are simultaneously synthesized on differentbeads, comprising: (a) forming a mixture comprising a plurality ofbeads; (b) separating the beads into subsets; (c) extending thenucleotide or oligonucleotide sequence on the surface of the beads byadding an individual nucleotide via chemical synthesis; (d) pooling thesubsets of beads in (c) into a single common pool; (e) repeating steps(b), (c) and (d) multiple times to produce combinatorially a thousand ormore nucleotide or oligonucleotide sequences; and (f) collecting thenucleotide- or oligonucleotide-adorned beads.
 12. A method forsimultaneously preparing a thousand or more nucleotide- oroligonucleotide-adorned beads wherein a uniform or near-uniformnucleotide or oligonucleotide sequence is synthesized upon anyindividual bead while a plurality of different nucleotide oroligonucleotide sequences are simultaneously synthesized on differentbeads, comprising: (a) forming a mixture comprising a plurality ofbeads; (b) separating the beads into subsets; (c) extending thenucleotide or oligonucleotide sequence on the surface of the beads byadding an individual nucleotide via chemical synthesis; (d) pooling thesubsets of beads in (c) into a single common pool; (e) repeating steps(b), (c) and (d) multiple times to produce a combinatorially largenumber of nucleotide or oligonucleotide sequences; and (f) collectingthe nucleotide- or oligonucleotide-adorned beads; (g) performingpolynucleotide synthesis on the surface of the plurality of beads in apool-and-split synthesis, such that in each cycle of synthesis the beadsare split into a plurality of subsets wherein each subset is subjectedto different chemical reactions; (h) repeating the pool-and-splitsynthesis multiple times.
 113. The method of claim 112, wherein thenucleotide or oligonucleotide sequence on the surface of the bead is amolecular barcode; or the pool-and-split synthesis steps occur every2-10 cycles, rather than every cycle; or the barcode contains built-inerror correction; or -p1 the barcode ranges from 4 to 1000 nucleotidesin length; or the polynucleotide synthesis is phosphoramidite synthesis;or the polynucleotide synthesis is reverse direction phosphoramiditechemistry; or each subset is subjected to a different nucleotide; or themethod further comprises one or more subsets receive a cocktail of twonucleotides; or each subset is subjected to a different canonicalnucleotide; or the bead is a microbead; or the bead is a nanoparticle;or the bead is a macrobead; or the oligonucleotide barcoded bead is adinucleotide; or the oligonucleotide barcoded bead is a trinucleotide;or the pool-and-split synthesis is repeated twelve times; or thediameter of the complexed bead is from 10 μm to 95 μm.
 114. An apparatusfor creating a composite single-cell sequencing library via amicrofluidic system, comprising: an oil-surfactant inlet comprising afilter and a carrier fluid channel, wherein said carrier fluid channelfurther comprises a resistor; an inlet for an analyte comprising afilter and a carrier fluid channel, wherein said carrier fluid channelfurther comprises a resistor; an inlet for mRNA capture microbeads andlysis reagent comprising a filter and a carrier fluid channel, whereinsaid carrier fluid channel further comprises a resistor; said carrierfluid channels have a carrier fluid flowing therein at an adjustable orpredetermined flow rate; wherein each said carrier fluid channels mergeat a junction; and said junction being connected to a mixer, whichcontains an outlet for drops.
 115. The apparatus of claim 114, whereinthe analyte comprises a chemical reagent, a protein, a drug, anantibody, an enzyme, a nucleic acid, an organelle; a cell or anycombination thereof; or said junction is connected to said mixer by afluid carrier channel with a constriction for droplet pinch-off; or theanalyte is a cell; or the analyte is a mammalian cell; or the cell is abrain cell; or the cell is a retina cell; or the cell is a human bonemarrow cell; or the cell is a host-pathogen cell the analyte is complextissue; or the lysis reagent comprises an anionic surfactant, such assodium lauroyl sarcosine, or a chaotropic salt, such as guanidiuniumthiocyanate; or the filter comprises square PDMS; or the resistor isserpentine having a length from 7000 9000, width of 50-75 μm and depthof 100-150 mm; or the resistor has a diameter of 50 μm; or the channelshaving a length of length of 8000-12,000 μm and width of 12.5-250 mm,and depth of 100-150 mm; or wherein the channel has a diameter of 125μm; or wherein the mixer has a length of 7000-9000 μm and a width of110-140 μm; or wherein the mixer width is 125 μm; or the oil-surfactantis a PEG block polymer; or the carrier fluid is water-glycerol mixture.